documents: FDA-2013-N-0581-0002

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0581-0002 FDA FDA-2013-N-0581 Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems for Acute Coronary Syndrome, Cardiac and Non- Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for Intra-Aortic Balloon and Control Systems for Septic Shock or Pulsatile Flow Generation Rule Final Rule 2013-12-30T05:00:00Z 2013 12 2013-12-30T05:00:00Z   2013-12-30T14:52:49Z 2013-31218 0 0 09000064814e1976

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