AVIVO Mobile Patient Management (MPM) System

AVIVO Mobile Patient Management (MPM) System is an FDA 510(k)-cleared medical device (K153160) manufactured by Medtronic, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 29, 2016. Regulation: 8.