MODEL 885 INFUSION PUMP, MODIFICATION

MODEL 885 INFUSION PUMP, MODIFICATION is an FDA 510(k)-cleared medical device (K924872) 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 16, 1993. Regulation: 8.