documents: FDA-2013-N-1518-0004

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2013-N-1518-0004 FDA FDA-2013-N-1518 Reference -1 FDA Circulatory System Devices Panel of the Medical Devices Advisory Committee Meeting, December 5-6, 2012 re Cardiovascular Devices; Reclassification of Nonroller-Type Cardiopulmonary Bypass Blood Pumps for Cardiopulmonary and Circulatory Bypass; Effective Date of Requirement for Premarket Approval for Nonroller-Type Cardiopulmonary Bypass Blood Pumps for Temporary Ventricular Supporting & Related Material Background Material 2015-06-08T04:00:00Z 2015 6     2015-06-08T16:13:41Z   0 0 0900006481b22510

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