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documents: FDA-2016-D-2565-0010

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2016-D-2565-0010 FDA FDA-2016-D-2565 510(k) Third-Party Review Program; Draft Guidance for Industry, Food and Drug Administration Staff, and Third-Party Review Organizations; Availability Notice Notice of Availability 2018-09-14T04:00:00Z 2018 9 2018-09-14T04:00:00Z 2018-12-14T04:59:59Z 2018-12-14T02:04:21Z 2018-19992 0 0 09000064836ee543

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