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withdrawn,object_id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
FDA-2017-P-5124-0003,FDA,FDA-2017-P-5124,Medical Devices; Exemption From Premarket Notification: Over-the-Counter Denture Repair Kits,Notice,Announcement,2017-11-20T05:00:00Z,2017,11,2017-11-20T05:00:00Z,2018-01-20T04:59:59Z,2017-11-20T15:01:06Z,2017-25065,0,0,0900006482c9142c
FDA-2017-P-5124-0001,FDA,FDA-2017-P-5124,"Citizen Petition from Hyman, Phelps & McNamara, PC",Other,Citizen Petition,2017-08-23T04:00:00Z,2017,8,2017-08-23T04:00:00Z,2018-02-20T04:59:59Z,2017-08-23T12:10:51Z,,0,0,0900006482a9619d
FDA-2017-P-5124-0002,FDA,FDA-2017-P-5124,"Acknowledgement Letter from FDA DDM to Hyman, Phelps & McNamara, PC",Other,Acknowledgement Letter/Receipt,2017-08-23T04:00:00Z,2017,8,2017-08-23T04:00:00Z,,2017-08-23T12:10:57Z,,0,0,0900006482a961a1