MAXI-TORQUE PLUS SOFTIP ANGIOGRAPHIC CATHETER

MAXI-TORQUE PLUS SOFTIP ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K963092) manufactured by Adam Spencer 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 12, 1997. Regulation: 8.