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Final rule 2025-21955

Medical Devices; Quality Management System Regulation Technical Amendments

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.

Source: FederalRegister.gov API v1Recently refreshed. Last successful refresh: 2026-07-31 22:49:02 UTC.

Source-supplied record

Document details

Document number
2025-21955
Published
Dec 4, 2025
Effective
Feb 2, 2026
Comments close
Not supplied
Federal Register citation
90 FR 55978

Docket identifiers

  • Docket No. FDA-2025-N-4635

CFR references

  • Title 21, part 801
  • Title 21, part 803
  • Title 21, part 812
  • Title 21, part 860
  • Title 21, part 862
  • Title 21, part 864
  • Title 21, part 866
  • Title 21, part 868
  • Title 21, part 872
  • Title 21, part 874
  • Title 21, part 876
  • Title 21, part 878
  • Title 21, part 880
  • Title 21, part 882
  • Title 21, part 886
  • Title 21, part 888
  • Title 21, part 890
  • Title 21, part 892