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withdrawn,object_id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-2016-N-0969-0004,FDA,FDA-2016-N-0969,Revocation of Authorization of Emergency Use of an In Vitro Diagnostic Device for Detection of Zika Virus,Notice,Announcement,2017-06-30T04:00:00Z,2017,6,2017-06-30T04:00:00Z,,2017-06-30T15:20:29Z,2017-13666,0,0,09000064827c0422
FDA-2016-N-0969-0003,FDA,FDA-2016-N-0969,"Authorization of Emergency Use of an In Vitro Diagnostic Device for
Detection of Zika Virus; Availability",Notice,Announcement,2016-12-20T05:00:00Z,2016,12,2016-12-20T05:00:00Z,,2016-12-20T14:59:56Z,2016-30532,0,0,090000648242960c
FDA-2016-N-0969-0002,FDA,FDA-2016-N-0969,"Authorization of Emergency Use of an In Vitro Diagnostic Device for
Detection of Zika Virus; Availability",Notice,Announcement,2016-04-22T04:00:00Z,2016,4,2016-04-22T04:00:00Z,,2016-04-22T14:32:43Z,2016-09370,0,0,0900006481f833c6
FDA-2016-N-0969-0001,FDA,FDA-2016-N-0969,"Authorization of Emergency Use of an In Vitro Diagnostic Device for
Diagnosis of Zika Virus Infection; Availability",Notice,Announcement,2016-03-28T04:00:00Z,2016,3,2016-03-28T04:00:00Z,,2016-03-30T19:51:23Z,2016-06888,0,0,0900006481ee3c01