Megapulse III Shortwave Diathermy

Megapulse III Shortwave Diathermy is an FDA 510(k)-cleared medical device (K153456) manufactured by Accelerated Care Plus. 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 13, 2016. Regulation: 8.