MERIT MEDICAL SYSTEMS, INC., GUIDE WIRE TORQUE DEVICE

MERIT MEDICAL SYSTEMS, INC., GUIDE WIRE TORQUE DEVICE is an FDA 510(k)-cleared medical device (K072552) manufactured by Merit Medical Systems, 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 December 13, 2007. Regulation: 8.