NIHON KOHDEN ELECTROENCEPHALOGRAPH

NIHON KOHDEN ELECTROENCEPHALOGRAPH is an FDA 510(k)-cleared medical device (K944678) 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 May 21, 1995. Regulation: 8.