BRAINMASTER 2E MODULE AND SOFTWARE BIOFEEDBACK DEVICE

BRAINMASTER 2E MODULE AND SOFTWARE BIOFEEDBACK DEVICE is an FDA 510(k)-cleared medical device (K990538) manufactured by Brainmaster. 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 18, 1999. Regulation: 8.