PROSTHESIS, VASCULAR BIFURCATED

PROSTHESIS, VASCULAR BIFURCATED is an FDA 510(k)-cleared medical device (K760130) manufactured by Usci, Div. C.R. Bard, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 1976. Regulation: 8.