MD-2 IONTOPHORESIS UNIT

MD-2 IONTOPHORESIS UNIT is an FDA 510(k)-cleared medical device (K895365) manufactured by R. A. Fischer Co. Corp.. 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 June 25, 1990. Regulation: 8.