ViperCath XC Peripheral Exchange Catheter

ViperCath XC Peripheral Exchange Catheter is an FDA 510(k)-cleared medical device (K183000) manufactured by Cardiovascular Systems, 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 December 28, 2018. Regulation: 8.