MODIFICATIONS TO CORDIS' SUPER FLOW CATHETERS

MODIFICATIONS TO CORDIS' SUPER FLOW CATHETERS is an FDA 510(k)-cleared medical device (K862244) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 24, 1986. Regulation: 8.