Medical devices in the United States must undergo a review process by the Food and Drug Administration before they can be marketed for patient use.
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Similar to drugs, medical devices in the United States go through a review process by the US Food and Drug Administration (FDA) before they can be marketed for use in patients.
Jill Jin (Tue,) reported a other. Medical devices in the United States must undergo a review process by the Food and Drug Administration before they can be marketed for patient use.