DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE

DYNAPHOR(TM) 101, IONTOPHORESIS DEVICE is an FDA 510(k)-cleared medical device (K894549) 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 February 8, 1990. Regulation: 8.