MASTERSCREEN CPX AND OXYCON CPX

MASTERSCREEN CPX AND OXYCON CPX is an FDA 510(k)-cleared medical device (K040698) manufactured by Viasys Healthcare GmbH. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 6, 2004. Regulation: 8.