DIATHERMY DEVICE-MICROFOCUS

DIATHERMY DEVICE-MICROFOCUS is an FDA 510(k)-cleared medical device (K941567) manufactured by Cheung Laboratories, Inc.. 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 April 21, 1996. Regulation: 8.