INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE

INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE is an FDA 510(k)-cleared medical device (K924009) manufactured by Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard. 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 5, 1992. Regulation: 8.