NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON

NOVAMETRIX MODEL 1265 END TIDAL CARBON DIOXIDE MON is an FDA 510(k)-cleared medical device (K910019) manufactured by Novametrix Medical Systems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 25, 1991. Regulation: 8.