BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30

BIOFEEDBACK TMG1, 4, BIO1, PA1, 2, BA1/BA30 is an FDA 510(k)-cleared medical device (K884850) 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 February 1, 1989. Regulation: 8.