USCI LINX EZ GUIDE WIRE EXTENSION W/PRO/PEL COAT

USCI LINX EZ GUIDE WIRE EXTENSION W/PRO/PEL COAT is an FDA 510(k)-cleared medical device (K920980) 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 August 23, 1992. Regulation: 8.