documents: FDA-2021-N-0507-0084
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0507-0084 | FDA | FDA-2021-N-0507 | Reference 1 - ISO 13485:2016, ‘‘Medical devices - Quality management systems -Requirements for regulatory purposes,’’ 3rd Ed., March 1, 2016. | Supporting & Related Material | Background Material | 2024-02-02T05:00:00Z | 2024 | 2 | 2024-02-03T14:07:18Z | 0 | 0 | 09000064863d82d7 |
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