Federal Register: FDA Reclassifies Vascular Autograft Storage Solutions to Reduce Regulatory Burdens
September 30, 2026
September 30, 2026
WASHINGTON, Sept. 30 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following action in the Federal Register.
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Medical Devices; Gastroenterology-Urology Devices; Classification of the Flushing and Storage Solution for Vascular Autografts at Room Temperature
The Food and Drug Administration (FDA) is classifying the flushing and storage solution for vascular autografts at room temperature into class II . . .
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Medical Devices; Gastroenterology-Urology Devices; Classification of the Flushing and Storage Solution for Vascular Autografts at Room Temperature
The Food and Drug Administration (FDA) is classifying the flushing and storage solution for vascular autografts at room temperature into class II . . .