TERUMO SURFLO I.V. CATHETER

TERUMO SURFLO I.V. CATHETER is an FDA 510(k)-cleared medical device (K133280) manufactured by Terumo (Philippines) Corporation. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 11, 2014. Regulation: 8.