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Radiology devices branch on the move

This article was originally published in The Gray Sheet

Executive Summary

FDA's Radiological Devices Branch is moving from its current home in the Office of Device Evaluation to the Office of In Vitro Diagnostic Device Evaluation and Safety (OIVD), FDA says. One of the center's largest review branches, the radiological devices office encompasses diagnostic devices such as x-ray and magnetic resonance imaging equipment, as well as non-diagnostic products such as radiofrequency ablation catheters and cancer radiation treatments. The branch is expected to retain its current personnel, according to a member of the Radiological Society of North America
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