DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM

DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM is an FDA 510(k)-cleared medical device (K001629) manufactured by Disetronic Medical Systems AG. 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 20, 2000. Regulation: 8.