MODIFICATION TO PLUM XL INFUSION PUMP

MODIFICATION TO PLUM XL INFUSION PUMP is an FDA 510(k)-cleared medical device (K010924) manufactured by Abbott Laboratories. 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 5, 2001. Regulation: 8.