BD Prevue™ II Peripheral Vascular Access System

BD Prevue™ II Peripheral Vascular Access System is an FDA 510(k)-cleared medical device (K240146) manufactured by Bard Access Systems, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 17, 2024. Regulation: 8.