C02 MONITOR-OIR-7101

C02 MONITOR-OIR-7101 is an FDA 510(k)-cleared medical device (K841498) 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 May 13, 1984. Regulation: 8.