documents: FDA-2017-D-6841-0017
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-6841-0017 | FDA | FDA-2017-D-6841 | Unique Device Identification: Policy Regarding Compliance Dates for Class I and Unclassified Devices, Direct Marking, and Global Unique Device Identification Database Requirements for Certain Devices; Guidance for Industry and Food and Drug Administration Staff; Availability | Rule | Final Rule | 2022-07-25T04:00:00Z | 2022 | 7 | 2022-07-25T04:00:00Z | 2022-07-25T15:42:10Z | 2022-15828 | 0 | 0 | 09000064851e551d |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref