3F ANGIOPTIC ANGIOGRAPHIC CATHETER

3F ANGIOPTIC ANGIOGRAPHIC CATHETER is an FDA 510(k)-cleared medical device (K964033) manufactured by AngioDynamics, 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 May 5, 1997. Regulation: 8.