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documents: FDA-2022-N-0790-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-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

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