ALARIS SYSTEM WITH MMS, MODEL 8XXX

ALARIS SYSTEM WITH MMS, MODEL 8XXX is an FDA 510(k)-cleared medical device (K072105) manufactured by Cardinal Health 303,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 December 27, 2007. Regulation: 8.