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withdrawn,object_id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-2022-N-3207-0001,FDA,FDA-2022-N-3207,"Medical Devices; Gastroenterology-Urology Devices; Classification of the
Gastrointestinal Lesion SoftwareDetection System",Rule,Direct Final Rule,2023-01-03T05:00:00Z,2023,1,2023-01-03T05:00:00Z,,2023-01-04T15:40:56Z,2022-28494,0,0,090000648557e719