RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM

RE-TRAKE WEISS EMERGENCY AIRWAY & THORACIC SYSTEM is an FDA 510(k)-cleared medical device (K862909) manufactured by Intl. Medical Devices , Ltd.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 8, 1986. Regulation: 8.