HI-TORQUE PROGRESS GUIDE WIRE FAMILY

HI-TORQUE PROGRESS GUIDE WIRE FAMILY is an FDA 510(k)-cleared medical device (K091825) manufactured by Abbott Vascular, 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 September 24, 2009. Regulation: 8.