SKINTACT ECG ELECTRODES WITH KL 02 LIQUID GEL

SKINTACT ECG ELECTRODES WITH KL 02 LIQUID GEL is an FDA 510(k)-cleared medical device (K024247) manufactured by Leonhard Lang GmbH. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 2003. Regulation: 8.