USCI(R) SILK (TM) GUIDE WIRE

USCI(R) SILK (TM) GUIDE WIRE is an FDA 510(k)-cleared medical device (K903923) 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 November 20, 1990. Regulation: 8.