DYNATRON 300 ULRASOUND

DYNATRON 300 ULRASOUND is an FDA 510(k)-cleared medical device (K920939) manufactured by Dynatronics Laser Corp.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 1993. Regulation: 8.