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Zdrowie i gospodarka · 02/08/2019

FDA Releases Draft Guidance for Medical Device Testing in Magnetic Resonance Environment

The Food and Drug Administration (FDA) has released a draft guidance document outlining recommendations for testing and labeling medical devices to ensure safety in the Magnetic Resonance (MR) environment, with the goal of promoting consistency in reviews and testing across various medical devices.

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