EXPANSION OF THE CORDIS PTA DILATATION CATHETER

EXPANSION OF THE CORDIS PTA DILATATION CATHETER is an FDA 510(k)-cleared medical device (K894899) 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 January 25, 1990. Regulation: 8.