FOAM ECG ELECTRODE, 2060 AND 2061

FOAM ECG ELECTRODE, 2060 AND 2061 is an FDA 510(k)-cleared medical device (K770988) manufactured by Cardio-Dynamics Laboratories, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 13, 1977. Regulation: 8.