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withdrawn,object_id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-0794-0001,FDA,FDA-2022-N-0794,"General and Plastic Surgery Devices; Reclassification of Optical Diagnostic Devices for Melanoma Detection and Electrical Impedance Spectrometers, To Be Renamed Computer-Aided Devices Which Provide Adjunctive Diagnostic Information About Lesions Suspicious for Melanoma",Proposed Rule,Amendment,2022-06-30T04:00:00Z,2022,6,2022-06-30T04:00:00Z,2022-08-30T03:59:59Z,2022-08-31T01:01:03Z,2022-13954,0,0,09000064851ab45e