Medical Device Classification Procedures; Change of Address; Technical Amendment
Information
Type
Rule
Regulated products
Medical Devices
Published
August 21, 2017
Last updated
August 21, 2017
Description
Document number 2017-17564. 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.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)