DYNATRON 200 MICROCURRENT

DYNATRON 200 MICROCURRENT is an FDA 510(k)-cleared medical device (K903577) manufactured by Dynatronics 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 March 14, 1991. Regulation: 8.