documents: FDA-2019-N-5192-0014
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2019-N-5192-0014 | FDA | FDA-2019-N-5192 | Microbiology Devices; Reclassification of Human Immunodeficiency Virus Serological Diagnostic and Supplemental Tests and Human Immunodeficiency Virus Nucleic Acid Diagnostic and Supplemental Tests | Rule | Final Rule | 2022-05-16T04:00:00Z | 2022 | 5 | 2022-05-16T04:00:00Z | 2022-05-16T14:35:27Z | 2022-10461 | 0 | 0 | 090000648507f151 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref