SKINTACT MULTIFUNCTION ELECTRODES, MODEL DF 21

SKINTACT MULTIFUNCTION ELECTRODES, MODEL DF 21 is an FDA 510(k)-cleared medical device (K041883) manufactured by Leonhard Lang GmbH. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 6, 2004. Regulation: 8.