documents: FDA-2026-N-6733-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2026-N-6733-0001 | FDA | FDA-2026-N-6733 | Medical Devices; Immunology and Microbiology Devices; Classification of the Over-the-Counter Test To Detect SARS-CoV-2 From Clinical Specimens | Rule | Final Rule | 2026-07-24T04:00:00Z | 2026 | 7 | 2026-07-24T04:00:00Z | 2026-07-24T19:13:16Z | 2026-14985 | 0 | 0 | 09000064b93be761 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref