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withdrawn,object_id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-2014-N-0440-0015,FDA,FDA-2014-N-0440,Microbiology Devices: Reclassification of Influenza Virus Antigen Detection Test Systems Intended for Use Directly With Clinical Specimens,Rule,Final Rule,2017-01-12T05:00:00Z,2017,1,2017-01-12T05:00:00Z,,2017-01-12T16:17:02Z,2017-00199,0,0,0900006482463233
FDA-2014-N-0440-0001,FDA,FDA-2014-N-0440,Microbiology Devices; Reclassification of Influenza Virus Antigen Detection Test Systems Intended for Use Directly With Clinical Specimens,Proposed Rule,Notice of Proposed Rulemaking (NPRM),2014-05-22T04:00:00Z,2014,5,2014-05-22T04:00:00Z,2014-08-21T03:59:59Z,2014-08-21T01:03:49Z,2014-11635,0,0,090000648170c5a0