documents: FDA-2017-D-6765-0005
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2017-D-6765-0005 | FDA | FDA-2017-D-6765 | Replacement Reagent and Instrument Family Policy for In Vitro Diagnostic Devices; Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2022-08-17T04:00:00Z | 2022 | 8 | 2022-08-17T04:00:00Z | 2022-08-17T12:11:22Z | 2022-17643 | 0 | 0 | 090000648524485a |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref