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withdrawn,object_id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-0790-0001,FDA,FDA-2022-N-0790,Medical Devices; Gastroenterology Urology Devices; Classification of the Non-Implanted Electrical Stimulation Device for Management of Premature Ejaculation,Rule,Final Rule,2022-06-06T04:00:00Z,2022,6,2022-06-06T04:00:00Z,,2022-06-07T12:10:56Z,2022-12082,0,0,0900006485141286