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withdrawn,object_id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-P-5124-0005,FDA,FDA-2017-P-5124,Medical Devices: Exemption from Premarket Notification; Class II Devices; Over-the-Counter Denture Repair Kit,Rule,Final Rule,2018-03-14T04:00:00Z,2018,3,2018-03-14T04:00:00Z,,2018-03-14T14:20:53Z,2018-05116,0,0,090000648300e7c9
FDA-2017-P-5124-0004,FDA,FDA-2017-P-5124,"Final Response Letter from FDA to Hyman, Phelps & McNamara, PC",Other,Response(s),2018-02-07T05:00:00Z,2018,2,2018-02-07T05:00:00Z,,2018-02-07T16:03:47Z,,0,0,0900006482ef71e5