BIOFEEDBACK ELECTROENCEPHALOGRAPH/ELECTROMYOGRAPH

BIOFEEDBACK ELECTROENCEPHALOGRAPH/ELECTROMYOGRAPH is an FDA 510(k)-cleared medical device (K894510) manufactured by Capscan Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 1990. Regulation: 8.