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withdrawn,object_id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-0195-0001,FDA,FDA-2013-N-0195,Effective Date of Requirement for Premarket Approval for Three Class III Preamendments Devices: Reclassification of Sorbent Hemoperfusion Devices for the Treatment of Poisoning and Drug Overdose,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2013-04-04T04:00:00Z,2013,4,2013-04-04T04:00:00Z,2013-05-07T03:59:59Z,2014-05-07T01:03:54Z,2013-07730,0,0,0900006481268b15