documents: FDA-2013-N-1518-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-1518-0002 FDA FDA-2013-N-1518 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 Support Rule Final Rule 2015-06-08T04:00:00Z 2015 6 2015-06-08T04:00:00Z   2015-06-08T14:41:30Z 2015-13889 0 0 0900006481b210e7

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