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Zdrowie i gospodarka · 21.08.2017

Medical Device Classification Procedures; Change of Address; Technical Amendment

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.

Source: Federal Register — Food and Drug AdministrationOpen original release →