CURAPULS 403 DIATHERMY UNIT

CURAPULS 403 DIATHERMY UNIT is an FDA 510(k)-cleared medical device (K900189) manufactured by Henley Intl.. 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 September 17, 1990. Regulation: 8.