HOSPIRA PLUM A+ INFUSION PUMP, MODEL 12391

HOSPIRA PLUM A+ INFUSION PUMP, MODEL 12391 is an FDA 510(k)-cleared medical device (K070398) manufactured by Hospira, Inc.. 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 April 23, 2007. Regulation: 8.