HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE

HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE is an FDA 510(k)-cleared medical device (K060449) manufactured by Guidant Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 29, 2006. Regulation: 8.