ALARIS PC UNIT MODULE 8000 WITH SOFTWARE CORRECTION

ALARIS PC UNIT MODULE 8000 WITH SOFTWARE CORRECTION is an FDA 510(k)-cleared medical device (K110535) manufactured by Carefusion 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 March 25, 2012. Regulation: 8.