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withdrawn,object_id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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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,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