DYNATRON 350 EMG/BIOFEEDBACK ANALYZER

DYNATRON 350 EMG/BIOFEEDBACK ANALYZER is an FDA 510(k)-cleared medical device (K900639) manufactured by Dynatronics Laser 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 October 3, 1990. Regulation: 8.