ELECTROENCEPHALOGRAPHS EEG-5208,5210

ELECTROENCEPHALOGRAPHS EEG-5208,5210 is an FDA 510(k)-cleared medical device (K820066) 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 February 3, 1982. Regulation: 8.