
Applied Vascular
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AVD INTIMAX (TM) BILIARY CATHETER is an FDA 510(k)-cleared medical device (K910006) manufactured by Applied Vascular. 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 February 12, 1991. Regulation: 8.