TRANSIT/RAPIDTRANSIT/SPEEDSTER/PROWLER INFUSION CATHETER

TRANSIT/RAPIDTRANSIT/SPEEDSTER/PROWLER INFUSION CATHETER is an FDA 510(k)-cleared medical device (K972518) 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 November 3, 1997. Regulation: 8.