CURAPULS 419 DIATHERMY UNIT

CURAPULS 419 DIATHERMY UNIT is an FDA 510(k)-cleared medical device (K861248) 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 May 29, 1986. Regulation: 8.