BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR

BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR is an FDA 510(k)-cleared medical device (K884849) manufactured by Moe. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 1989. Regulation: 8.