documents: FDA-2017-D-5625-0015

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-D-5625-0015 FDA FDA-2017-D-5625 Recommendations for Dual 510(k) and Clinical Laboratory Improvement Amendments Waiver by Application Studies; Guidance for Industry and Food and Drug Administration Staff; Availability Notice Notice of Data Availability 2020-02-26T05:00:00Z 2020 2 2020-02-26T05:00:00Z   2020-02-26T15:03:25Z 2020-03859 0 0 09000064843b4ec8

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