ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE

ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE is an FDA 510(k)-cleared medical device (K980119) manufactured by Guidant Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1998. Regulation: 8.