documents: FDA-2019-N-5610-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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

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