documents: FDA-2025-N-1264-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2025-N-1264-0001 FDA FDA-2025-N-1264 Medical Devices; Hematology and Pathology Devices; Classification of the Fluorescence In Situ Hybridization-Based Detection of Chromosomal Abnormalities From Patients With Hematologic Malignancies Rule Final Rule 2025-06-26T04:00:00Z 2025 6 2025-06-26T04:00:00Z   2025-06-26T17:27:00Z 2025-11793 0 0 09000064b8e322d7

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