ASE MAXI-TORQUE, SUPPLE FLEX ANGIOGRAPHIC CATHETERS

ASE MAXI-TORQUE, SUPPLE FLEX ANGIOGRAPHIC CATHETERS is an FDA 510(k)-cleared medical device (K950855) 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 May 29, 1995. Regulation: 8.