documents: FDA-2011-D-0652-0033

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2011-D-0652-0033 FDA FDA-2011-D-0652 The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)]; Guidance for Industry and Food and Drug Administra tion Staff Other Guidance 2014-07-28T04:00:00Z 2014 7 2014-07-28T04:00:00Z   2024-11-12T05:27:17Z   1 0 09000064817e7e24

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