MONITOR, PATIENT, RESP. CARBON DIOXIDE

MONITOR, PATIENT, RESP. CARBON DIOXIDE is an FDA 510(k)-cleared medical device (K770713) manufactured by Cavitron Corp.. 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 26, 1977. Regulation: 8.