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documents: FDA-2019-N-5192-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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

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