KADIR HI-TORQUE GUIDE WIRE

KADIR HI-TORQUE GUIDE WIRE is an FDA 510(k)-cleared medical device (K871297) manufactured by Argon Medical Corp.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 9, 1987. Regulation: 8.