documents: FDA-2021-N-0600-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2021-N-0600-0001 | FDA | FDA-2021-N-0600 | Medical Devices; Cardiovascular Devices; Classification of the Intravascular Bleed Monitor | Rule | Final Rule | 2022-06-08T04:00:00Z | 2022 | 6 | 2022-06-08T04:00:00Z | 2022-06-08T13:55:34Z | 2022-12364 | 0 | 0 | 090000648514d1b2 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref