documents: FDA-2007-D-0025-0004
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2007-D-0025-0004 | FDA | FDA-2007-D-0025 | Guidance for Industry and the Food and Drug Administration; Modifications to Devices Subject to Premarket Approval--the Premarket Approval Supplement Decisionmaking Process; Availability | Notice | NAD-Notice of Availability of Data | 2008-12-11T05:00:00Z | 2008 | 12 | 2008-12-11T12:59:15Z | 2008-12-21T02:37:29Z | E8-29330 | 0 | 0 | 09000064807d702e |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref