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withdrawn,object_id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-N-5610-0001,FDA,FDA-2019-N-5610,"Medical Devices; Radiology Devices; Classification of the Radiological
Computer-Assisted Diagnostic Software for Lesions Suspicious for Cancer",Rule,Final Rule,2020-01-22T05:00:00Z,2020,1,2020-01-22T05:00:00Z,,2020-01-22T14:50:10Z,2020-00497,0,0,09000064842d3ad7