329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR

329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR is an FDA 510(k)-cleared medical device (K852253) 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 28, 1985. Regulation: 8.