documents: FDA-2019-N-5192-0004
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-5192-0004 | FDA | FDA-2019-N-5192 | Reference 3 - BPAC-07.18.18-07.19.18-Meeting-Issue-Summary-Reclassification-of-HIV-Point-of-Care-and-Laboratory-based-serological-and-NAT-diagnostic-devices re: Microbiology Devices; Reclassification of Human Immunodeficiency Virus Serological Diagnostic and Supplemental Tests and Human Immunodeficiency Virus Nucleic Acid Diagnostic and Supplemental Tests | Supporting & Related Material | Background Material | 2020-02-21T05:00:00Z | 2020 | 2 | 2020-02-24T00:10:37Z | 0 | 0 | 0900006484399cd0 |
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- 0 rows from regs_document_id in fr_regs_crossref