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documents: FDA-2026-N-9911-0001

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2026-N-9911-0001 FDA FDA-2026-N-9911 Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Anti-Tumor Necrosis Factor Alpha Monoclonal Antibody Test System for Inflammatory Bowel Disease Rule Final Rule 2026-09-10T04:00:00Z 2026 9 2026-09-10T04:00:00Z   2026-09-10T17:09:11Z 2026-18430 0 0 09000064b9511a93

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