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withdrawn,object_id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
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