USCI 8F EXTRA LARGE LUMEN GUIDE CATHETER

USCI 8F EXTRA LARGE LUMEN GUIDE CATHETER is an FDA 510(k)-cleared medical device (K884502) manufactured by 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 January 17, 1989. Regulation: 8.