CORDIS POWERFLEX PLUS PTA BALLOON CATHETER

CORDIS POWERFLEX PLUS PTA BALLOON CATHETER is an FDA 510(k)-cleared medical device (K971516) 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 July 22, 1997. Regulation: 8.