home / openregs / dockets

dockets: FDA-2003-P-0346

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

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-2003-P-0346 FDA 513(f) Reclassification Petition for In Vitro Diagnostics for Anti-Hepatitis A Virus IgM and Total Antibodies Nonrulemaking 2021-09-01T01:03:10Z 0b00006480496d39   CLOSED DATE: 03/13/2006 Docket Status: CLOSED     ["Total Antibodies", "Anti-Hepatitis A Virus IgM", "In Vitro Diagnostics", "513(f)", "RECLASSIFICATION PETITION", "CDRH"] CDRH 513(f) Reclassification Petition for In Vitro Diagnostics for Anti-Hepatitis A Virus IgM and Total Antibodies     {"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": "shortTitle", "label": "Short Title", "tooltip": "A combination of letters and or numbers assigned to an agency's regulatory action for purposes of brevity."}], "keywords": ["Total Antibodies", "Anti-Hepatitis A Virus IgM", "In Vitro Diagnostics", "513(f)", "RECLASSIFICATION PETITION", "CDRH"], "modifyDate": "2021-09-01T01:03:10Z", "dkAbstract": "CLOSED DATE: 03/13/2006\r\nDocket Status: CLOSED", "agencyId": "FDA", "program": "CDRH", "shortTitle": "513(f) Reclassification Petition for In Vitro Diagnostics for Anti-Hepatitis A Virus IgM and Total Antibodies", "subType2": null, "title": "513(f) Reclassification Petition for In Vitro Diagnostics for Anti-Hepatitis A Virus IgM and Total Antibodies", "generic": "P", "field1": null, "docketType": "Nonrulemaking", "petitionNbr": null, "rin": null, "organization": null, "legacyId": "2003P-0564", "subType": null, "category": null, "field2": null, "effectiveDate": null, "objectId": "0b00006480496d39"} single_get

Links from other tables

  • 5 rows from docket_id in documents
Powered by Datasette · Queries took 0.248ms · Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API · Privacy