USCI ANGIOGRAPHIC BALLOON CATHETER

USCI ANGIOGRAPHIC BALLOON CATHETER is an FDA 510(k)-cleared medical device (K831854) 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 October 19, 1983. Regulation: 8.