ELCTROCARDIOGRAPH, EK-6

ELCTROCARDIOGRAPH, EK-6 is an FDA 510(k)-cleared medical device (K760265) manufactured by Burdick Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 22, 1976. Regulation: 8.