documents: FDA-2017-D-6535-0016

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-6535-0016 FDA FDA-2017-D-6535 Reference 7 - Appropriate Use of Voluntary Consensus Standards in Premarket Submissions for Medical Devices; Guidance for Industry and Food and Drug Administration Staff RE: Standards Development and the Use of Standards in Regulatory Submissions Reviewed in the Center for Biologics Evaluation and Research Guidance for Industry Supporting & Related Material Background Material 2019-03-26T04:00:00Z 2019 3     2019-03-26T15:31:28Z   0 0 0900006483b2fa0f

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