888 ARTERIAL/VENOUS CATHETER INTRODUCER

888 ARTERIAL/VENOUS CATHETER INTRODUCER is an FDA 510(k)-cleared medical device (K771982) manufactured by Usci, Div. 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 November 1, 1977. Regulation: 8.