CAV 3.0C SOFTWARE PROGRAM

CAV 3.0C SOFTWARE PROGRAM is an FDA 510(k)-cleared medical device (K890932) manufactured by Siemens Life Support Systems. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 11, 1989. Regulation: 8.