EKG, ECG KENZ, ECG 303

EKG, ECG KENZ, ECG 303 is an FDA 510(k)-cleared medical device (K896772) manufactured by Cambridge Medical Instruments, 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 February 25, 1990. Regulation: 8.