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The Food and Drug Administration (FDA, the Agency, or we) is amending certain medical device regulations to revise references and language in existing Code of Federal Regulations (CFR) provisions to conform with the final rule "Medical Devices; Quality System Regulation Amendments" (QMSR Final Rule). This rule does not impose any new requirements on affected parties. This action is editorial in nature to correct errors, conform regulatory references, and ensure accuracy and clarity in the Agency's regulations.
Published
Dec 4, 2025
Effective
Feb 2, 2026
Citation
90 FR 55978
Agencies
2
Full text not available in our database.
View on Federal Register →Get a plain-English explanation of what this regulation does, which agencies are responsible, and how it affects existing rules.
No document text available yet
Docket No. FDA-2025-N-4635
21 CFR 801
21 CFR 803
21 CFR 812
21 CFR 860
21 CFR 862
21 CFR 864
21 CFR 866
21 CFR 868
21 CFR 872
21 CFR 874
21 CFR 876
21 CFR 878
21 CFR 880
21 CFR 882
21 CFR 886
21 CFR 888
21 CFR 890
21 CFR 892