Health and Human Services Department Docket FDA-2013-N-1529 Final Rule

2017-17564: Medical Device Classification Procedures; Change of Address; Technical Amendment

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Summary

The Food and Drug Administration (FDA or Agency) is amending the Medical Device Classification Procedures regulation to reflect a change in address for the Center for Devices and Radiological Health (CDRH). This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.

The agency’s own summary, as published.

What this changes

Amends 1 part of the Code of Federal Regulations — the standing rules this notice rewrites.

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