documents: FDA-2017-D-6765-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2017-D-6765-0001 | FDA | FDA-2017-D-6765 | Replacement Reagent and Instrument Family Policy for In Vitro Diagnostic Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability | Notice | Notice of Availability | 2017-12-18T05:00:00Z | 2017 | 12 | 2017-12-18T05:00:00Z | 2018-03-20T03:59:59Z | 2018-03-21T01:01:16Z | 2017-27132 | 0 | 0 | 0900006482d30212 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref