DESERET ANGIO-GUIDE LARGE VEIN CATH.

DESERET ANGIO-GUIDE LARGE VEIN CATH. is an FDA 510(k)-cleared medical device (K833092) manufactured by Warner-Lambert Co.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1983. Regulation: 8.