MODEL AO-800PA CO2 MODULE

MODEL AO-800PA CO2 MODULE is an FDA 510(k)-cleared medical device (K894691) manufactured by Nihon Kohden America, 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 December 21, 1989. Regulation: 8.