PULSED GALVANIC STIMULATOR, 450-DYNAMAX

PULSED GALVANIC STIMULATOR, 450-DYNAMAX is an FDA 510(k)-cleared medical device (K801053) manufactured by U.S. Medical 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 June 3, 1980. Regulation: 8.