VICKERS MEDICAL MODEL 112 TREONIC DC2

VICKERS MEDICAL MODEL 112 TREONIC DC2 is an FDA 510(k)-cleared medical device (K791645) manufactured by Vickers America Medical Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 1, 1979. Regulation: 8.