DUPEL II BUFFERED IONTOPHORESIS ELECTRODES

DUPEL II BUFFERED IONTOPHORESIS ELECTRODES is an FDA 510(k)-cleared medical device (K970491) manufactured by Empi. 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, 1997. Regulation: 8.