QUINTON MODEL 630 AND 636 ECG DATA CART

QUINTON MODEL 630 AND 636 ECG DATA CART is an FDA 510(k)-cleared medical device (K791364) manufactured by Quinton, 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 August 2, 1979. Regulation: 8.