SURESET 3.0 ML RESERVOIR, MODEL 24-103

SURESET 3.0 ML RESERVOIR, MODEL 24-103 is an FDA 510(k)-cleared medical device (K024056) manufactured by Applied Diabetes Research, Incorporated. 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 January 16, 2003. Regulation: 8.