CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL

CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL is an FDA 510(k)-cleared medical device (K811539) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 30, 1981. Regulation: 8.