MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER

MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K955111) manufactured by Adam Spence 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 January 30, 1996. Regulation: 8.