SEQUE INFUSION CATHETER (S-25,30,35,40,45,50,60)

SEQUE INFUSION CATHETER (S-25,30,35,40,45,50,60) is an FDA 510(k)-cleared medical device (K955534) manufactured by International Innovations, 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 July 31, 1996. Regulation: 8.