STRATO/INFUSAID PERIPORT INFUSION SET 41770,41771

STRATO/INFUSAID PERIPORT INFUSION SET 41770,41771 is an FDA 510(k)-cleared medical device (K960391) manufactured by Strato/Infusaid, Inc.. 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 July 2, 1996. Regulation: 8.