HOSPIRA MEDNET MEDICATION MANAGEMENT SUITE

HOSPIRA MEDNET MEDICATION MANAGEMENT SUITE is an FDA 510(k)-cleared medical device (K141102) 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 July 7, 2014. Regulation: 8.