AVIVO Mobile Patient Management (MPM) System
K-Number: K153160 · 2016-03-30
ApplicantMedtronic, Inc.
Decision Date2016-03-30
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
AVIVO Mobile Patient Management (MPM) System is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2016-03-30 under approval number K153160. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the AVIVO Mobile Patient Management (MPM) System?
AVIVO Mobile Patient Management (MPM) System is a medical device that received FDA 510(k) clearance on 2016-03-30. It is manufactured by Medtronic, Inc.. The 510(k) number is K153160.
When was AVIVO Mobile Patient Management (MPM) System approved by the FDA?
AVIVO Mobile Patient Management (MPM) System received FDA 510(k) clearance on 2016-03-30, under approval number K153160.
What company makes AVIVO Mobile Patient Management (MPM) System?
AVIVO Mobile Patient Management (MPM) System is manufactured by Medtronic, Inc..
What is the FDA product code for AVIVO Mobile Patient Management (MPM) System?
The FDA product code for AVIVO Mobile Patient Management (MPM) System is MHX.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.