CORDIS ENCOR PERVENOUS ATRIAL & VENTRICULAR LEADS

CORDIS ENCOR PERVENOUS ATRIAL & VENTRICULAR LEADS is an FDA 510(k)-cleared medical device (K844970) 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 March 26, 1985. Regulation: 8.