dockets: FDA-2013-P-1611
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | title | docket_type | last_modified | object_id | rin | dkabstract | category | subtype | keywords | program | short_title | effective_date | organization | attrs_raw | attr_source |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-2013-P-1611 | FDA | Amend two Regulations Within The Code of Federal Regulations, Title 21 - Food and Drugs, Chapter 1, Supchapter H- Medical Devices, Part 872- Dental Devices (Subpart D-Prosthetic Devices 872.3690 - Tooth Shade Resin Material and Subpart G-Miscellaneous Devices 872.6070 - Ultraviolet Activator for Polymerization) to Include Special Controls Guidance | Nonrulemaking | 2024-07-25T08:45:32Z | 0b000064814ba6f5 | CLOSED | ["CDRH", "Citizen Petition", "2013-10154", "Special ControlsGuidance", "Prosthetic Devices", "Miscellaneous Devices", "bisphenol-A glycidyl methacrylate", "CLOSED"] | CDRH | Amend Subpart D-Prosthetic Devices 872.3690 - Tooth Shade Resin Material and Subpart G-Miscellaneous Devices 872.6070 - Ultraviolet Activator for Polymerization to Include Special Controls Guidance | {"displayProperties": [{"name": "abstract", "label": "General Information", "tooltip": "Describes an agency's specific regulatory action; equivalents: Abstract, Description, Docket Subject, Related To, Summary."}, {"name": "legacyId", "label": "Legacy ID", "tooltip": "A pre-FDMS agency specific identifier migrated from a legacy system."}, {"name": "generic", "label": "Docket Item Code", "tooltip": "An agency specific code that identifies the type of document that established the docket (regulatory action)."}, {"name": "program", "label": "Center", "tooltip": "The agency specific program associated with the docket (regulatory action); equivalents: Docket Item Code, Location."}, {"name": "field2", "label": "Docket Status", "tooltip": "Used to Identity that a Docket's Status is Open or Closed"}, {"name": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["CDRH", "Citizen Petition", "2013-10154", "Special ControlsGuidance", "Prosthetic Devices", "Miscellaneous Devices", "bisphenol-A glycidyl methacrylate", "CLOSED"], "modifyDate": "2024-07-25T08:45:32Z", "dkAbstract": "CLOSED", "agencyId": "FDA", "program": "CDRH", "shortTitle": "Amend Subpart D-Prosthetic Devices 872.3690 - Tooth Shade Resin Material and Subpart G-Miscellaneous Devices 872.6070 - Ultraviolet Activator for Polymerization to Include Special Controls Guidance", "subType2": null, "title": "Amend two Regulations Within The Code of Federal Regulations, Title 21 - Food and Drugs, Chapter 1, Supchapter H- Medical Devices, Part 872- Dental Devices (Subpart D-Prosthetic Devices 872.3690 - Tooth Shade Resin Material and Subpart G-Miscellaneous Devices 872.6070 - Ultraviolet Activator for Polymerization) to Include Special Controls Guidance", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2013-10154", "subType": null, "category": null, "field2": "CLOSED", "effectiveDate": null, "objectId": "0b000064814ba6f5"} | single_get |
Links from other tables
- 5 rows from docket_id in documents