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documents: FDA-2025-N-1210-0002

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2025-N-1210-0002 FDA FDA-2025-N-1210 Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Postmarket Surveillance of Medical Devices Notice 30 Day Proposed Information Collection 2025-12-23T05:00:00Z 2025 12 2025-12-23T05:00:00Z 2026-01-22T04:59:59Z 2026-01-24T13:18:31Z 2025-23630 0 0 09000064b91065e6

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