Passeo-35 Xeo Peripheral Dilatation Catheter

Passeo-35 Xeo Peripheral Dilatation Catheter is an FDA 510(k)-cleared medical device (K222065) manufactured by Biotronik, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 15, 2023. Regulation: 8.