documents: FDA-2025-N-2424-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2025-N-2424-0001 FDA FDA-2025-N-2424 Medical Devices; Immunology and Microbiology Devices; Classification of the Mutation Detection Test for Myeloproliferative Neoplasms Rule Final Rule 2025-08-21T04:00:00Z 2025 8     2025-08-21T17:44:12Z 2025-16038 0 0 09000064b8f0b275

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