CORDIS VENTRICULAR ANTECHAMBER (VA)

CORDIS VENTRICULAR ANTECHAMBER (VA) is an FDA 510(k)-cleared medical device (K955832) manufactured by Cordis Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 1996. Regulation: 8.