PROWLER PLUS INFUSION CATHETER

PROWLER PLUS INFUSION CATHETER is an FDA 510(k)-cleared medical device (K993266) manufactured by Cordis Neurovascular, 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 October 27, 1999. Regulation: 8.