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Applied Diabetes Research, Incorporated
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SURESET INFUSION SET, MODEL 8023 is an FDA 510(k)-cleared medical device (K012429) 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 November 5, 2001. Regulation: 8.

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