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withdrawn,object_id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-2019-P-3347-0006,FDA,FDA-2019-P-3347,Medical Devices; Exemption From Premarket Notification; Class II Devices; Powered Wheeled Stretcher,Rule,Final Rule,2020-01-14T05:00:00Z,2020,1,2020-01-14T05:00:00Z,,2020-04-13T16:50:57Z,2020-00295,0,0,090000648429e1b6
FDA-2019-P-3347-0005,FDA,FDA-2019-P-3347,Petition Response Letter from FDA CDRH to Stryker Medical,Other,Agency Response,2020-01-07T05:00:00Z,2020,1,2020-01-07T05:00:00Z,,2020-01-07T15:08:59Z,,0,0,0900006484276af7