TRAUMAFUSE RAPID INFUSION DEVICE

TRAUMAFUSE RAPID INFUSION DEVICE is an FDA 510(k)-cleared medical device (K890077) manufactured by The Traumafuse Co.. 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 2, 1989. Regulation: 8.