MODEL 880 INFUSION PUMP, MODIFICATION

MODEL 880 INFUSION PUMP, MODIFICATION is an FDA 510(k)-cleared medical device (K924871) manufactured by 3M Health Care, Ltd.. 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 17, 1993. Regulation: 8.