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withdrawn,object_id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-2017-N-6538-0080,FDA,FDA-2017-N-6538,"Obstetrical and Gynecological Devices; Reclassification of Single-Use  Female Condom, To Be Renamed Single-Use Internal Condom",Rule,Final Rule,2018-09-27T04:00:00Z,2018,9,2018-09-27T04:00:00Z,,2018-09-27T14:41:04Z,2018-21044,0,0,090000648377a070
FDA-2017-N-6538-0001,FDA,FDA-2017-N-6538,"Obstetrical and Gynecological Devices; Reclassification of Single-Use
Female Condom, To Be Renamed Single-Use Internal Condom",Proposed Rule,Notice of Proposed Rulemaking (NPRM),2017-12-04T05:00:00Z,2017,12,2017-12-04T05:00:00Z,2018-02-03T04:59:59Z,2018-02-03T02:01:42Z,2017-26011,0,0,0900006482cd3c3c