MODEL EEG-4217 ELECTROENCEPHALOGRAPH

MODEL EEG-4217 ELECTROENCEPHALOGRAPH is an FDA 510(k)-cleared medical device (K791234) manufactured by Nihon Kohden America, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 11, 1979. Regulation: 8.