Skip to the page

Data / Federal rules / Blood

Federal rules on blood: 10 since September 2024

7 final rules and 3 proposed rules since September 5, 2024, 1 of them marked significant. Most come from the Food and Drug Administration (7), Food Safety and Inspection Service (3).

SpecStream is the live web data engine for teams and agents. It reads every rule and proposed rule in the Federal Register each morning, and this page is that reading. Name your industry once and new rules, comment deadlines and effective dates arrive in your sheet, CRM, Slack or agent as they are published.

Every document, newest first

DocumentAgencyTypePublished
Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product
2026-16727
Food and Drug AdministrationFinal ruleAug 17
Medical Devices; Hematology and Pathology Devices; Classification of the Von Willebrand Factor Assay
2026-10898
Food and Drug AdministrationFinal ruleJun 1
Visual Post-Mortem Inspection in Swine Slaughter Establishments
2026-10186
Food Safety and Inspection ServiceFinal ruleMay 21
Maximum Line Speed Under the New Swine Slaughter Inspection System (NSIS)
2026-03228 · significant
Food Safety and Inspection ServiceProposed ruleFeb 19
Medical Devices; Quality Management System Regulation Technical Amendments
2025-21955
Food and Drug AdministrationFinal ruleDec 4, 2025
Visual Post-Mortem Inspection in Swine Slaughter Establishments
2025-15749
Food Safety and Inspection ServiceProposed ruleAug 19, 2025
Medical Devices; Hematology and Pathology Devices; Classification of the Fluorescence In Situ Hybridization-Based Detection of Chromosomal Abnormalities From Patients With Hematologic Malignancies
2025-11793
Food and Drug AdministrationFinal ruleJun 26, 2025
Hematology and Pathology Devices; Reclassification of In Situ Hybridization Test Systems for Use With a Corresponding Approved Oncology Therapeutic Product
2025-10549
Food and Drug AdministrationProposed ruleJun 11, 2025
Medical Devices; Hematology and Pathology Devices; Classification of the Coagulation System for the Measurement of Whole Blood Viscoelastic Properties in Perioperative Patients
2025-08151
Food and Drug AdministrationFinal ruleMay 9, 2025
Medical Devices; Hematology and Pathology Devices; Classification of the Heparin and Direct Oral Factor Xa Inhibitor Drug Test System
2024-19824
Food and Drug AdministrationFinal ruleSep 5, 2024

Other topics

Read from the Federal Register API, last updated 2026-10-23. The document on federalregister.gov is the official record; dates and dockets can change through later corrections. Free to reuse with credit to SpecStream under CC BY 4.0.