AG-820PA FI02 MODULE

AG-820PA FI02 MODULE is an FDA 510(k)-cleared medical device (K896359) 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 March 8, 1990. Regulation: 8.