BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER

BRAEMAR MODEL DL700 AMBULATORY ELECTROCARDIOGRAPHIC RECORDER is an FDA 510(k)-cleared medical device (K945130) manufactured by Braemar 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 April 11, 1995. Regulation: 8.