documents: FDA-2016-D-2565-0005

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2016-D-2565-0005 FDA FDA-2016-D-2565 Draft Guidance for Industry Food and Drug Administration Staff on 510(k) Third Party Review Program Other Guidance 2016-09-12T04:00:00Z 2016 9 2016-09-12T04:00:00Z   2024-11-07T23:49:36Z   1 0 09000064821f9e4c

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