USCI LUMISILK GUIDE WIRE WITH PRO/PEL COATING

USCI LUMISILK GUIDE WIRE WITH PRO/PEL COATING is an FDA 510(k)-cleared medical device (K925074) 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 February 28, 1993. Regulation: 8.