BARDEX I.C. LATEX FOLEY CATHETER

BARDEX I.C. LATEX FOLEY CATHETER is an FDA 510(k)-cleared medical device (K040658) manufactured by C.R. Bard, Inc.. 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 September 28, 2004. Regulation: 8.