documents: FDA-2011-D-0652-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2011-D-0652-0002 FDA FDA-2011-D-0652 Draft Guidance for Industry and Food and Drug Administration Staff The 510(k) Program Evaluating Substantial Equivalence in Premarket Notifications [510(k)] Other Guidance 2011-12-28T05:00:00Z 2011 12 2011-12-28T05:00:00Z 2012-04-27T03:59:59Z 2014-09-27T01:07:24Z   0 0 0900006480f8a513

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