ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE

ABDOMINAL AORTIC AND JUNCTIONAL TOURNIQUET (AAJT) DEVICE is an FDA 510(k)-cleared medical device (K133029) manufactured by Compression Works, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 5, 2013. Regulation: 8.