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102 rows where agency_id = "FDA", document_type = "Proposed Rule" and posted_year = 2012 sorted by posted_date descending
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| id | agency_id | docket_id | title | document_type | subtype | posted_date ▲ | posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2012-N-1067-0001 | FDA | FDA-2012-N-1067 | New Animal Drugs: Updating Tolerances for Residues of New Animal Drugs in Food | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-12-05T05:00:00Z | 2012 | 12 | 2012-12-05T05:00:00Z | 2013-03-06T04:59:59Z | 2013-03-06T03:02:58Z | 2012-29322 | 0 | 0 | 090000648117f7ca |
| FDA-1997-P-0007-0002 | FDA | Artificially Sweetened Fruit Jelly and Artificially Sweetened Fruit Preserves and Jams; Revocation of Standards of Identity FDA-1997-P-0007 | Revocation of Standards of Identity: Artificially Sweetened Fruit Jelly and Artificially Sweetened Fruit Preserves and Jams | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-12-04T05:00:00Z | 2012 | 12 | 2012-12-04T05:00:00Z | 2013-03-05T04:59:59Z | 2013-03-02T03:01:58Z | 2012-29181 | 0 | 0 | 090000648117e45c |
| FDA-2012-F-1100-0001 | FDA | FDA-2012-F-1100 | DSM Nutritional Products; Filing of Food Additive Petition (Animal Use) | Proposed Rule | Petition | 2012-12-04T05:00:00Z | 2012 | 12 | 2012-12-04T05:00:00Z | 2013-01-04T04:59:59Z | 2013-03-04T17:07:54Z | 2012-29202 | 0 | 0 | 090000648117e3e4 |
| FDA-1975-N-0269-0001 | FDA | Vinyl Chloride Polymers in Contact with Food- CLOSED FDA-1975-N-0269 | Vinyl Chloride Polymers in Contact With Food | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-12-04T05:00:00Z | 2012 | 12 | 2012-12-04T05:00:00Z | 1975-11-03T04:59:59Z | 2018-01-17T02:03:31Z | 75-23241 | 0 | 0 | 09000064805c6f3c |
| FDA-2012-N-1148-0001 | FDA | FDA-2012-N-1148 | Actions Related to Nicotine Replacement Therapies and Smoking-Cessation Products: Report to Congress on Innovative Products and Treatments for Tobacco Dependence; Public Hearing | Proposed Rule | Public Hearing | 2012-11-28T05:00:00Z | 2012 | 11 | 2012-11-28T05:00:00Z | 2013-01-03T04:59:59Z | 2013-09-09T01:02:00Z | 2012-28835 | 0 | 0 | 09000064811762a5 |
| FDA-2011-N-0090-0222 | FDA | FDA-2011-N-0090 | Unique Device Identification System; Amendment | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-11-19T05:00:00Z | 2012 | 11 | 2012-11-19T05:00:00Z | 2012-12-20T04:59:59Z | 2012-12-20T03:02:20Z | 2012-28015 | 0 | 0 | 090000648116ca95 |
| FDA-2004-C-0559-0001 | FDA | Cryovac North America, Filing of (CAP 4C0276) proposing that the color additive regulations be amended to provide for the safe use of as a color additive in or on cooked meat products FDA-2004-C-0559 | Withdrawal of Color Additive Petition: Cryovac North America | Proposed Rule | Withdrawal | 2012-10-25T04:00:00Z | 2012 | 10 | 2012-10-25T04:00:00Z | 2012-10-25T18:07:27Z | 2012-26242 | 0 | 0 | 090000648115036c | |
| FDA-1977-N-0259-0039 | FDA | Cultured & Acidified Buttermilk, Yogurts, Milks & Eggnog - OPEN FDA-1977-N-0259 | Cultured and Acidified Buttermilk, Yogurts, Cultured and Acidified Milks, and Eggnog; Proposal to Establish New Identity Standards; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2012-10-17T04:00:00Z | 2012 | 10 | 2012-10-17T04:00:00Z | 1977-10-11T03:59:59Z | 2019-02-25T15:48:45Z | 77-27221 | 0 | 0 | 09000064805ed1ee |
| FDA-2012-N-0447-0006 | FDA | FDA-2012-N-0447 | Antimicrobial Animal Drug Sales and Distribution Reporting: Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2012-09-26T04:00:00Z | 2012 | 9 | 2012-09-26T04:00:00Z | 2012-11-27T04:59:59Z | 2015-05-20T01:31:01Z | 2012-23740 | 0 | 0 | 0900006481128b32 |
| FDA-2011-N-0090-0019 | FDA | FDA-2011-N-0090 | Agency Information Collection Activities; Proposed Collection; Unique Device Identification System; Extension of Comment Period | Proposed Rule | Extension of Comment Period | 2012-09-17T04:00:00Z | 2012 | 9 | 2012-09-17T04:00:00Z | 2012-10-26T03:59:59Z | 2012-11-21T03:02:41Z | 2012-22821 | 0 | 0 | 09000064811196ad |
| FDA-2012-N-0780-0003 | FDA | FDA-2012-N-0780 | Regulatory New Drug Review: Solutions for Study Data Exchange Standards; Meeting; Request for Comments; Correction | Proposed Rule | Correction | 2012-09-17T04:00:00Z | 2012 | 9 | 2012-09-17T04:00:00Z | 2012-09-17T14:51:49Z | 2012-22793 | 0 | 0 | 0900006481119716 | |
| FDA-2011-N-0252-0002 | FDA | FDA-2011-N-0252 | Privacy Act, Exempt Record System | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-28T04:00:00Z | 2012 | 8 | 2012-08-28T04:00:00Z | 2012-11-14T04:59:59Z | 2012-11-13T03:08:15Z | 2012-20890 | 0 | 0 | 09000064810f47c3 |
| FDA-1978-N-1926-0001 | FDA | Dura Substitute FDA-1978-N-1926 | Classification of Dura Substitutes | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-22T04:00:00Z | 2012 | 8 | 2012-08-22T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-22T17:43:17Z | 0 | 0 | 090000648059e67e | |
| FDA-1978-N-0915-0001 | FDA | Preformed Craniosynostosis Strip FDA-1978-N-0915 | Classification of Preformed Craniosynostosis Strips - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-22T04:00:00Z | 2012 | 8 | 2012-08-22T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-22T17:31:19Z | 0 | 0 | 090000648058d47b | |
| FDA-1978-N-1927-0001 | FDA | Artificial Embolization Device FDA-1978-N-1927 | Classification of Artifical Embolization Devices | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-22T04:00:00Z | 2012 | 8 | 2012-08-22T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-22T18:05:08Z | 0 | 0 | 090000648059e68d | |
| FDA-1978-N-0928-0001 | FDA | Transcutaneous Electrical Nerve Stimulator for Pain Relief FDA-1978-N-0928 | Classification of Transcutaneous Electrical Nerve Stimulators for Pain Relief | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-22T04:00:00Z | 2012 | 8 | 2012-08-22T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-22T14:51:57Z | 0 | 0 | 090000648058de45 | |
| FDA-1978-N-1982-0001 | FDA | Central Nervous System Fluid Shunt & Components FDA-1978-N-1982 | Classification of Central Nervous System Fluid Shunts and Components - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T13:17:43Z | 0 | 0 | 09000064805a1b17 | |
| FDA-1978-N-0614-0001 | FDA | Preformed Nonalterable Cranioplasty Plate FDA-1978-N-0614 | Classification of Preformed Nonalterable Cranioplasty Plates | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T11:58:46Z | 0 | 0 | 0900006480577dfc | |
| FDA-1978-N-0360-0001 | FDA | Implanted Spinal Cord Stimulator for Bladder Evacuation FDA-1978-N-0360 | Classification of Implanted Spinal Cord Stimulators for Bladder Evacuation - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T18:54:42Z | 0 | 0 | 090000648056e51f | |
| FDA-1978-N-0913-0001 | FDA | Cranial Electrotherapy Stimulator FDA-1978-N-0913 | Classification of Cranial Electrotherpay Stimulators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T14:11:09Z | 0 | 0 | 090000648058d2d4 | |
| FDA-1978-N-0616-0001 | FDA | Implanted Neuromuscular Stimulator FDA-1978-N-0616 | Classification of Implanted Neuromuscular Stimulators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T19:26:16Z | 0 | 0 | 0900006480578094 | |
| FDA-1978-N-0358-0001 | FDA | Cranioplasty Plate Fastener FDA-1978-N-0358 | Classification of Cranioplasty Plate Fasteners | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-21T04:00:00Z | 2012 | 8 | 2012-08-21T04:00:00Z | 1979-01-30T04:59:59Z | 2012-08-21T12:47:05Z | 0 | 0 | 090000648056e4ee | |
| FDA-1978-N-0907-0001 | FDA | Isolated Kidney Perfusion Transport Systems FDA-1978-N-0907 | Classification of Isolated Kidney Perfusion Transport Systems - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-15T04:00:00Z | 2012 | 8 | 2012-08-15T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-15T16:32:37Z | 0 | 0 | 090000648058ce17 | |
| FDA-1978-N-0311-0001 | FDA | Sorbebt Regenerated Dialysate Delivery Systems Hemodialys FDA-1978-N-0311 | Classification of Sorbebt Regenerated Dialysate Delivery Systems Hemodialys - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-15T04:00:00Z | 2012 | 8 | 2012-08-15T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-15T12:21:52Z | 0 | 0 | 090000648056d501 | |
| FDA-1978-N-1164-0001 | FDA | Gastrointestinal Tubes & Accessories FDA-1978-N-1164 | Classification of Gastrointestinal Tubes & Accessories | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-15T04:00:00Z | 2012 | 8 | 2012-08-15T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-15T18:33:56Z | 0 | 0 | 0900006480598309 | |
| FDA-1978-N-0906-0001 | FDA | Peritoneal Dialysis Systems & Accessories FDA-1978-N-0906 | Classification of Peritoneal Dialysis Systems and Accessories - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-15T04:00:00Z | 2012 | 8 | 2012-08-15T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-15T14:35:25Z | 0 | 0 | 090000648058cd69 | |
| FDA-2012-S-0008-0001 | FDA | FDA-2012-S-0008 | See FDA-2012-N-0780-0001 | Proposed Rule | Correction | 2012-08-14T04:00:00Z | 2012 | 8 | 2012-08-14T04:00:00Z | 2012-08-14T03:59:59Z | 2013-01-17T00:13:23Z | 2012-19748 | 0 | 0 | 09000064810d4c05 |
| FDA-1978-N-1130-0001 | FDA | Ureteral Stents FDA-1978-N-1130 | Classification of Ureteral Stents | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-14T04:00:00Z | 2012 | 8 | 2012-08-14T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-14T13:19:16Z | 0 | 0 | 0900006480597a54 | |
| FDA-1978-N-1662-0001 | FDA | Electrohydraulic Lithotritors FDA-1978-N-1662 | Classification of Electrohydraulic Lithotritors | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-14T04:00:00Z | 2012 | 8 | 2012-08-14T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-14T15:49:58Z | 0 | 0 | 090000648059c604 | |
| FDA-1977-N-0031-0002 | FDA | Poisonous or Deleterious Substances-RETIRED FDA-1977-N-0031 | Poisonous or Deleterious Substances in Food - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-10T04:00:00Z | 2012 | 8 | 2012-08-10T04:00:00Z | 2012-08-15T02:01:11Z | 0 | 0 | 09000064805da4a2 | ||
| FDA-1978-N-1543-0001 | FDA | Chloramphenicol Ophthalmic Solution FDA-1978-N-1543 | Chloramphenicol Ophthalmic Solution; Deletion of Chemical Assay - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-06T04:00:00Z | 2012 | 8 | 2012-08-06T04:00:00Z | 2012-08-06T18:22:13Z | 0 | 0 | 090000648059bce2 | ||
| FDA-1978-N-0375-0001 | FDA | Medical Devices Classification of Prothrombin Time Tests-RETIRED FDA-1978-N-0375 | Medical Devices Classification of Prothrombin Time Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-08-01T04:00:00Z | 2012 | 8 | 2012-08-01T04:00:00Z | 1979-11-14T04:59:59Z | 2012-08-01T14:32:31Z | 0 | 0 | 090000648056e738 | |
| FDA-1978-N-0624-0001 | FDA | Medical Devices Classification of Prothrombin-Proconvertin Tests and Thrombotests-RETIRED FDA-1978-N-0624 | Medical Devices, Classification of Prothrombin-Proconvertin Tests and the Thrombotests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T15:24:39Z | 0 | 0 | 09000064805789e2 | |
| FDA-1978-N-1463-0001 | FDA | Processing Systems for Frozen Blood-RETIRED FDA-1978-N-1463 | Classification of Processing Systems for Frozen Blood | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T19:41:41Z | 0 | 0 | 090000648059b4ff | |
| FDA-1978-N-0625-0001 | FDA | Partial Thromboplastin Time Tests-RETIRED FDA-1978-N-0625 | Medical Devices Classification of Partial Thromboplastin Time Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T14:23:05Z | 0 | 0 | 0900006480578af1 | |
| FDA-1978-N-0381-0001 | FDA | Automated Cell Washing Centrifuges for Immuno-Hematology-RETIRED FDA-1978-N-0381 | Classifications of Automated Cell-Washing Centrifuges for Immuno-Hematology | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T20:05:30Z | 0 | 0 | 090000648056e831 | |
| FDA-2012-N-0447-0001 | FDA | FDA-2012-N-0447 | Antimicrobial Animal Drug Sales and Distribution Reporting | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 2012-09-26T03:59:59Z | 2012-10-02T02:01:15Z | 2012-18366 | 0 | 0 | 09000064810b436c |
| FDA-1978-N-1713-0001 | FDA | Blood & Plasma Warming Devices-RETIRED FDA-1978-N-1713 | Classification of Blood and Plasma Warming Devices | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T20:17:53Z | 0 | 0 | 090000648059cac0 | |
| FDA-1978-N-0382-0001 | FDA | Automated Coombs Test Systems-RETIRED FDA-1978-N-0382 | Classification of Automated Coombs Test Systems | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T19:55:20Z | 0 | 0 | 090000648056e845 | |
| FDA-1978-N-0124-0001 | FDA | Russell Viper Venom Reagent - RETIRED FDA-1978-N-0124 | Classification of Russell Viper Reagents | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T18:42:50Z | 0 | 0 | 0900006480564753 | |
| FDA-1978-N-0635-0001 | FDA | Empty Containers for the Collection & Processing of Blood-RETIRED FDA-1978-N-0635 | Classification of Containers for the Collection and Processing of Blood and Blood Components | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-27T04:00:00Z | 2012 | 7 | 2012-07-27T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T19:12:05Z | 0 | 0 | 09000064805792b9 | |
| FDA-1976-N-0302-0001 | FDA | Freedom of Information-RETIRED FDA-1976-N-0302 | Public Information - Notice of Proposed Rule Making | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-19T04:00:00Z | 2012 | 7 | 2012-07-19T04:00:00Z | 2012-08-10T02:01:09Z | 0 | 0 | 090000648051f9b1 | ||
| FDA-2012-F-0480-0002 | FDA | FDA-2012-F-0480 | Gruma Corp., Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filings of Food Additive Petition; Correction | Proposed Rule | Correction | 2012-07-18T04:00:00Z | 2012 | 7 | 2012-07-18T04:00:00Z | 2012-07-18T16:27:58Z | 2012-17432 | 0 | 0 | 090000648109fb3b | |
| FDA-1978-N-0929-0001 | FDA | Urological Tables & Accessories FDA-1978-N-0929 | Classification Urological Tables & Accessories - Notice of Proposed | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-17T04:00:00Z | 2012 | 7 | 2012-07-17T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-17T12:25:46Z | 0 | 0 | 090000648058defa | |
| FDA-2012-F-0728-0001 | FDA | FDA-2012-F-0728 | Filings of Food Additive Petitions: Representative Edward J. Markey | Proposed Rule | Petition | 2012-07-17T04:00:00Z | 2012 | 7 | 2012-07-17T04:00:00Z | 2012-09-18T03:59:59Z | 2012-09-18T02:01:14Z | 2012-17367 | 0 | 0 | 090000648109db7c |
| FDA-1978-N-1946-0001 | FDA | Classification of Ribdams FDA-1978-N-1946 | Classification of Ribdams - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-16T04:00:00Z | 2012 | 7 | 2012-07-16T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-16T19:57:56Z | 0 | 0 | 090000648059ee6a | |
| FDA-1978-N-1158-0001 | FDA | Urethral Dilators FDA-1978-N-1158 | Classification of Urethral Dilators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-16T04:00:00Z | 2012 | 7 | 2012-07-16T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-16T16:42:01Z | 0 | 0 | 0900006480598284 | |
| FDA-1978-N-1695-0001 | FDA | Nonimplanted Electrical Continence Devices FDA-1978-N-1695 | Classification of Nonimplanted Electrical Continence Devices - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-16T04:00:00Z | 2012 | 7 | 2012-07-16T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-16T20:12:54Z | 0 | 0 | 090000648059c891 | |
| FDA-1978-N-1957-0001 | FDA | Water Purification Systems for Hemodialysis FDA-1978-N-1957 | Classification of Water Purification Systems for Hemodialysis - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-16T04:00:00Z | 2012 | 7 | 2012-07-16T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-16T15:45:04Z | 0 | 0 | 090000648059f45b | |
| FDA-1978-N-1947-0001 | FDA | Protective Garments for Incontinence FDA-1978-N-1947 | Classification of Protective Garments for Incontinence - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-16T04:00:00Z | 2012 | 7 | 2012-07-16T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-17T02:01:12Z | 0 | 0 | 090000648059eeeb | |
| FDA-1978-N-0363-0001 | FDA | Gastroenterology-Urology Evacuators FDA-1978-N-0363 | Classification of Gastroenterology-Urology Evacuators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T13:14:10Z | 0 | 0 | 090000648056e5ab | |
| FDA-1978-N-1694-0001 | FDA | Hemodialyzers & Disposable Inserts (Kiil Type) FDA-1978-N-1694 | Classification of Hemodialyzers With Disposable Inserts - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-08-15T12:30:20Z | 0 | 0 | 090000648059c87f | |
| FDA-1978-N-1403-0001 | FDA | Water Jet Renal Stone Dislodger Systems FDA-1978-N-1403 | Classification of Water Jet Renal Stone Dislodger Systems - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T12:42:10Z | 0 | 0 | 090000648059b068 | |
| FDA-1978-N-1439-0001 | FDA | Blood Access Devices & Accessories FDA-1978-N-1439 | Classification of Blood Access Devices and Accessories - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T20:10:49Z | 0 | 0 | 090000648059b35a | |
| FDA-1978-N-0568-0001 | FDA | Urine Collectors & Accessories FDA-1978-N-0568 | Classification of Urine Collectors and Accessories - Notice of Proposed Rules | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T16:52:56Z | 0 | 0 | 0900006480575016 | |
| FDA-1978-N-1131-0001 | FDA | Colonic Irrigation Systems FDA-1978-N-1131 | Classification of Colonic Irrigation Systems - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T17:13:37Z | 0 | 0 | 0900006480597ad5 | |
| FDA-1978-N-1404-0001 | FDA | Urological Catheters & Accessories FDA-1978-N-1404 | Classification of Urological Catheters and Accessories - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T15:10:42Z | 0 | 0 | 090000648059b07c | |
| FDA-1978-N-0310-0001 | FDA | Mechanical Lithrotriptors FDA-1978-N-0310 | Classification of Mechanical Lithotriptors - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T14:12:44Z | 0 | 0 | 090000648056d481 | |
| FDA-1978-N-1972-0001 | FDA | Urological Clamps for Males FDA-1978-N-1972 | Classification of Urological Clamps for Males - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T15:34:28Z | 0 | 0 | 09000064805a1a79 | |
| FDA-1978-N-0871-0001 | FDA | Classification of Urethrotomes FDA-1978-N-0871 | Classification of Urethrotomes - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T14:51:50Z | 0 | 0 | 090000648058bbd9 | |
| FDA-1978-N-0064-0001 | FDA | Gastroenterology-Urology Surgical Instruments FDA-1978-N-0064 | Classification of Manual Gastroenterology-Urology Surgical Instruments and Accessories - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T13:31:08Z | 0 | 0 | 0900006480562416 | |
| FDA-1978-N-0569-0001 | FDA | Hemodialysis Systems & Accessories FDA-1978-N-0569 | Classification of Hemodialysis Systems & Accessories - Notice of Proposed Rules | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T18:47:33Z | 0 | 0 | 09000064805750cc | |
| FDA-1978-N-1501-0001 | FDA | Circumcision Instruments FDA-1978-N-1501 | Classification of Circumcision Instruments - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-13T04:00:00Z | 2012 | 7 | 2012-07-13T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-13T12:35:12Z | 0 | 0 | 090000648059b83e | |
| FDA-1978-N-1992-0001 | FDA | Testicular Prosthesis FDA-1978-N-1992 | Classification of Testicular Prostheses - Notice of Proposed Rule Making | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-12T04:00:00Z | 2012 | 7 | 2012-07-12T04:00:00Z | 1981-03-25T04:59:59Z | 2012-07-12T19:02:43Z | 0 | 0 | 09000064805a1bc8 | |
| FDA-2011-N-0090-0001 | FDA | FDA-2011-N-0090 | Unique Device Identification System | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-10T04:00:00Z | 2012 | 7 | 2012-07-10T04:00:00Z | 2012-11-08T04:59:59Z | 2012-12-18T03:02:50Z | 2012-16621 | 0 | 0 | 0900006481082634 |
| FDA-2012-N-0378-0001 | FDA | FDA-2012-N-0378 | Effective Date of Requirement for Premarket Approval for Shortwave Diathermy for All Other Uses | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-06T04:00:00Z | 2012 | 7 | 2012-07-06T04:00:00Z | 2012-10-05T03:59:59Z | 2014-11-30T01:49:58Z | 2012-16487 | 0 | 0 | 090000648107d286 |
| FDA-1978-N-0615-0001 | FDA | Implanted Cerebellar Stimulator FDA-1978-N-0615 | Classification of Implanted Cerebellar Stimulators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-03T04:00:00Z | 2012 | 7 | 2012-07-03T04:00:00Z | 1979-01-30T04:59:59Z | 2012-07-03T16:04:46Z | 0 | 0 | 0900006480577f62 | |
| FDA-1978-N-0628-0001 | FDA | Implanted Spinal Cord Stimulator for Pain Relief FDA-1978-N-0628 | Classification of Implanted Spinal Cord Stimulator for Pain Relief - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-03T04:00:00Z | 2012 | 7 | 2012-07-03T04:00:00Z | 1979-01-30T04:59:59Z | 2012-07-03T19:28:05Z | 0 | 0 | 0900006480578d5a | |
| FDA-1978-N-1962-0001 | FDA | Implanted Intracerebral/Subcortical Stimulator for Pain FDA-1978-N-1962 | Classification of Implanted Intracerebral/Subcortical Stimulators for Pain Relief - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-03T04:00:00Z | 2012 | 7 | 2012-07-03T04:00:00Z | 1979-01-30T04:59:59Z | 2012-07-03T16:47:10Z | 0 | 0 | 090000648059f4ab | |
| FDA-1978-N-0147-0001 | FDA | Implanted Peripheral Nerve Stimulator for Pain Relief FDA-1978-N-0147 | Classification of Implanted Peripheral Nerve Stimulators for Pain Relief - Notice of Proposal | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-03T04:00:00Z | 2012 | 7 | 2012-07-03T04:00:00Z | 1979-01-30T04:59:59Z | 2012-07-03T19:11:24Z | 0 | 0 | 0900006480565937 | |
| FDA-1978-N-0359-0001 | FDA | Implanted Diaphragmatic/Phrenic Nerve Stimulator FDA-1978-N-0359 | Classification of Implanted Diaphragmactic/Phrenic Nerve Stimulators - Notice of Proposed Rule | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-07-03T04:00:00Z | 2012 | 7 | 2012-07-03T04:00:00Z | 1979-01-30T04:59:59Z | 2012-07-03T16:24:26Z | 0 | 0 | 090000648056e50c | |
| FDA-1977-N-0411-0001 | FDA | Relationship of Methadone Treatment Programs FDA-1977-N-0411 | New Drugs - Notice of Proposal | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-28T04:00:00Z | 2012 | 6 | 2012-06-28T04:00:00Z | 2012-06-28T18:25:13Z | 0 | 0 | 09000064805ef214 | ||
| FDA-1977-N-0320-0001 | FDA | Protein Supplements-RETIRED FDA-1977-N-0320 | Protein Supplements Warning Labeling | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-27T04:00:00Z | 2012 | 6 | 2012-06-27T04:00:00Z | 1978-01-04T04:59:59Z | 2012-07-27T02:01:22Z | 0 | 0 | 09000064805ee04c | |
| FDA-1978-N-0924-0001 | FDA | Thrombin Time Test-RETIRED FDA-1978-N-0924 | Medical Devices Classification of Thrombin Time Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-26T04:00:00Z | 2012 | 6 | 2012-06-26T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-26T14:07:49Z | 0 | 0 | 090000648058db47 | |
| FDA-1978-N-0632-0001 | FDA | Thromboplastin Generation Test-RETIRED FDA-1978-N-0632 | Medical Devices Classification of Thromboplastin Generation Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-26T04:00:00Z | 2012 | 6 | 2012-06-26T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T17:19:05Z | 0 | 0 | 0900006480579039 | |
| FDA-1978-N-0061-0001 | FDA | Hematology and Pathology Devices Classification of Sickle Cell Tests-RETIRED FDA-1978-N-0061 | Medical Devices, Classification of Sickle Cell Tests | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-26T04:00:00Z | 2012 | 6 | 2012-06-26T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-03T23:00:56Z | 0 | 0 | 09000064805622e7 | |
| FDA-1978-N-0633-0001 | FDA | Automated Blood Grouping & Antibody Test Systems-RETIRED FDA-1978-N-0633 | Classification of Automated Blood Grouping and Antibody Test Systems | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T19:28:06Z | 0 | 0 | 09000064805790c6 | |
| FDA-1978-N-0368-0002 | FDA | Hematology Stains-RETIRED FDA-1978-N-0368 | Medical Devices Classification of Hematology Stains | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-19T02:01:17Z | 0 | 0 | 0900006481064007 | |
| FDA-1978-N-0379-0001 | FDA | Classification of Blood Mixing Devices & Blood Weighing Devices-RETIRED FDA-1978-N-0379 | Classification o Blood Mixing Devices and Blood Weighing Devices | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T19:18:26Z | 0 | 0 | 090000648056e7ec | |
| FDA-1978-N-0380-0001 | FDA | Automated Blood Cell Separators-RETIRED FDA-1978-N-0380 | Classification of Automated Blood Cell Separators | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-30T15:40:00Z | 0 | 0 | 090000648056e802 | |
| FDA-1978-N-0925-0001 | FDA | Calibrators for Cell Indices-RETIRED FDA-1978-N-0925 | Classification of Calibrators for Cell Indices | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T17:20:38Z | 0 | 0 | 090000648058dc33 | |
| FDA-1978-N-0123-0001 | FDA | Hematology Quality Control Mixtures FDA-1978-N-0123 | Medical Devices Classification of Hematology Quality Control Mixtures | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-25T18:30:01Z | 0 | 0 | 09000064805646b4 | |
| FDA-1978-N-1975-0001 | FDA | Red Cell Lysing Reagents -RETIRED FDA-1978-N-1975 | Medical Devices Classification of Red Cell Lysing Reagents | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-25T04:00:00Z | 2012 | 6 | 2012-06-25T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-25T18:19:43Z | 0 | 0 | 09000064805a1aaa | |
| FDA-1978-N-0622-0001 | FDA | Calibrators for Red Cell & White Cell Counting FDA-1978-N-0622 | Classification of Calibrators for Red Cell and White Cell Counting | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-22T04:00:00Z | 2012 | 6 | 2012-06-22T04:00:00Z | 1979-11-14T04:59:59Z | 2012-07-27T18:49:47Z | 0 | 0 | 09000064805787a1 | |
| FDA-1977-N-0259-0001 | FDA | Cultured & Acidified Buttermilk, Yogurts, Milks & Eggnog - OPEN FDA-1977-N-0259 | Cultured and Acidified Buttermilk, Yogurts, Cultured and Acidified Milks, and Eggnog, Proposal to Establish New Identity Standards | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-22T04:00:00Z | 2012 | 6 | 2012-06-22T04:00:00Z | 1977-09-09T03:59:59Z | 2019-03-24T00:09:39Z | 77-16126 | 0 | 0 | 09000064805ed17d |
| FDA-1978-N-1451-0001 | FDA | Blood Cell Diluents-RETIRED FDA-1978-N-1451 | Medical Devices Classification of Blood Cell Diluents | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-22T04:00:00Z | 2012 | 6 | 2012-06-22T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-22T20:29:14Z | 0 | 0 | 090000648059b43b | |
| FDA-1978-N-1177-0001 | FDA | Calibrators for Platelet Counting-RETIRED FDA-1978-N-1177 | Medical Devices, Classification of Calibrators for Platelet Counting | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-22T04:00:00Z | 2012 | 6 | 2012-06-22T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-22T17:09:05Z | 0 | 0 | 09000064805984fb | |
| FDA-1978-N-0115-0001 | FDA | Calibrators for Hemoglobin & Hematocrit Measurement-RETIRED FDA-1978-N-0115 | Classification of Calibrators for Hemoglobin and Hematocrit Measurement | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-22T04:00:00Z | 2012 | 6 | 2012-06-22T04:00:00Z | 1979-11-14T04:59:59Z | 2012-06-22T16:46:20Z | 0 | 0 | 0900006480564158 | |
| FDA-1979-N-0424-0001 | FDA | Labels of Drug & Cosmetic Products-RETIRED FDA-1979-N-0424 | Labels of Drug and Cosmetic Products; Proposal Regarding Placement of Required Information | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-20T04:00:00Z | 2012 | 6 | 2012-06-20T04:00:00Z | 2019-08-22T14:45:53Z | 74-15738 | 0 | 0 | 0900006480556490 | |
| FDA-1995-N-0302-0001 | FDA | Revocation of Certain Regulations "Reinventing Government" FDA-1995-N-0302 | Revocation of Certain Regulations; Opportunity for Public Comment | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-20T04:00:00Z | 2012 | 6 | 2012-06-20T04:00:00Z | 1996-01-12T04:59:59Z | 2024-07-26T20:50:02Z | 0 | 0 | 0900006480599974 | |
| FDA-2012-N-0303-0002 | FDA | FDA-2012-N-0303 | Gastroenterology Urology Devices Reclassification of Implanted Blood Access Devices | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-06-20T04:00:00Z | 2012 | 6 | 2012-06-20T04:00:00Z | 2012-09-19T03:59:59Z | 2013-08-28T01:02:25Z | 2012-15024 | 0 | 0 | 090000648105a25e |
| FDA-2012-N-0303-0001 | FDA | FDA-2012-N-0303 | Gastroenterology Urology Devices Reclassification of Implanted Blood Access Devices | Proposed Rule | 2012-06-20T00:00:00Z | 2012 | 6 | 2012-06-20T16:11:16Z | 0 | 1 | 09000064810594af | ||||
| FDA-2012-F-0480-0001 | FDA | FDA-2012-F-0480 | Gruma Corporation, Spina Bifida Association, March of Dimes Foundation, American Academy of Pediatrics, Royal DSM N.V., and National Council of La Raza; Filing of Food Additive Petition | Proposed Rule | Petition | 2012-06-13T04:00:00Z | 2012 | 6 | 2012-06-13T04:00:00Z | 2012-06-13T17:13:56Z | 2012-14263 | 0 | 0 | 0900006481047254 | |
| FDA-1981-N-0083-0001 | FDA | Potassium Bisulfite & Sulfite-CLOSED FDA-1981-N-0083 | Sulfiting Agents; Proposed Affirmation of GRAS Status With Specific Limitations; Removal From GRAS Status as Direct Human Food Ingredient | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-05-02T04:00:00Z | 2012 | 5 | 2012-05-02T04:00:00Z | 1982-09-10T03:59:59Z | 2013-02-12T03:00:56Z | 47 | 0 | 0 | 09000064805af57f |
| FDA-1994-N-0362-0002 | FDA | Quinine treatment/prevention of Malaria for OTC Human Use - CLOSED FDA-1994-N-0362 | Drug Products Containing Quinine for the Treatment and/or Prevention of Malaria for Over-The-Counter Human Use | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-04-06T04:00:00Z | 2012 | 4 | 2012-04-06T04:00:00Z | 1995-07-04T03:59:59Z | 2012-04-06T15:38:17Z | 95-9701 | 0 | 0 | 0900006480508547 |
| FDA-2012-N-0205-0002 | FDA | FDA-2012-N-0205 | Agreements and Memoranda of Understanding with Other Departments, Agencies, and Organizations | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-03-23T04:00:00Z | 2012 | 3 | 2012-03-23T04:00:00Z | 2012-06-07T03:59:59Z | 2012-06-06T02:00:50Z | 2012-06969 | 0 | 0 | 0900006480fdf3b9 |
| FDA-2009-N-0582-0055 | FDA | FDA-2009-N-0582 | Direct-to-Consumer Prescription Drug Advertisements; Presentation of the Major Statement in Television and Radio Advertisements in a Clear, Conspicuous, and Neutral Manner; Reopening of the Comment Period | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-03-23T04:00:00Z | 2012 | 3 | 2012-03-23T04:00:00Z | 2012-04-10T03:59:59Z | 2023-10-25T16:01:08Z | 2012-06948 | 0 | 0 | 0900006480fdf3d2 |
| FDA-2012-N-0159-0001 | FDA | FDA-2012-N-0159 | Microbiology Devices: Reclassification of Nucleic Acid-Based Systems for Mycobacterium tuberculosis Complex | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-03-19T04:00:00Z | 2012 | 3 | 2012-03-19T04:00:00Z | 2012-06-19T03:59:59Z | 2013-06-25T01:24:58Z | 2012-06518 | 0 | 0 | 0900006480fdacbe |
| FDA-2012-M-0076-0001 | FDA | FDA-2012-M-0076 | Gastroenterology-Urology Devices: Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose, etc. | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-02-17T05:00:00Z | 2012 | 2 | 2012-02-17T05:00:00Z | 2012-05-18T03:59:59Z | 2012-05-18T02:00:53Z | 2012-03810 | 0 | 0 | 0900006480fb8fc9 |
| FDA-2009-N-0582-0040 | FDA | FDA-2009-N-0582 | Direct-to-Consumer Prescription Drug Advertisements; Presentation of the Major Statement in Television and Radio Advertisements in a Clear, Conspicuous, and Neutral Manner; Notice of Availability of Study Data | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2012-01-27T05:00:00Z | 2012 | 1 | 2012-01-27T05:00:00Z | 2012-02-28T04:59:59Z | 2023-10-25T16:02:27Z | 2012-01672 | 0 | 0 | 0900006480fa7047 |
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id TEXT PRIMARY KEY,
agency_id TEXT,
docket_id TEXT REFERENCES dockets(id),
title TEXT,
document_type TEXT,
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posted_date TEXT,
posted_year INTEGER,
posted_month INTEGER,
comment_start_date TEXT,
comment_end_date TEXT,
last_modified TEXT,
fr_doc_num TEXT,
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CREATE INDEX idx_docs_docket ON documents(docket_id);
CREATE INDEX idx_docs_date ON documents(posted_date);
CREATE INDEX idx_docs_year ON documents(posted_year);
CREATE INDEX idx_docs_type ON documents(document_type);
CREATE INDEX idx_docs_frnum ON documents(fr_doc_num);