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withdrawn,object_id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-3185-0001,FDA,FDA-2022-N-3185,Medical Devices; Cardiovascular Devices; Classification of the Interventional Cardiovascular Implant Simulation Software Device,Rule,Final Rule,2022-12-28T05:00:00Z,2022,12,2022-12-28T05:00:00Z,,2022-12-29T17:40:46Z,2022-28173,0,0,090000648555aaf0