documents: FDA-2017-N-5153-0001

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-N-5153-0001 FDA FDA-2017-N-5153 Medical Devices; Gastroenterology-Urology Devices; Classification of the High Intensity Ultrasound System for Prostate Tissue Ablation Rule Final Rule 2017-10-02T04:00:00Z 2017 10 2017-10-02T04:00:00Z   2017-10-02T14:39:59Z 2017-21074 0 0 0900006482b8fda9

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