documents: FDA-2019-N-5192-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2019-N-5192-0001 | 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 | Proposed Rule | Notice of Proposed Rulemaking (NPRM) | 2020-02-21T05:00:00Z | 2020 | 2 | 2020-02-21T05:00:00Z | 2020-04-22T03:59:59Z | 2020-04-22T01:00:35Z | 2020-03515 | 0 | 0 | 0900006484397dd6 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref