NKA MODELS AB-601G AND AB-621G

NKA MODELS AB-601G AND AB-621G is an FDA 510(k)-cleared medical device (K900272) manufactured by Nihon Kohden America, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 30, 1990. Regulation: 8.