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documents: FDA-2013-N-0581-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-0581-0001 FDA FDA-2013-N-0581 Cardiovascular Devices; Reclassification of Intra-Aortic Balloon and Control Systems (IABP) for Acute Coronary Syndrome, Cardiac and Non-Cardiac Surgery, or Complications of Heart Failure; Effective Date of Requirement for Premarket Approval for IABP for Other Specific Intended Uses Proposed Rule Notice of Proposed Rulemaking (NPRM) 2013-06-19T04:00:00Z 2013 6 2013-06-19T04:00:00Z 2013-09-18T03:59:59Z 2014-01-14T13:53:46Z 2013-14553 0 0 0900006481331179

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