AVIVO Mobile Patient Management (MPM) System
K-Number: K153160 · 2016-03-30
Device Summary
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. The listed applicant is Medtronic, Inc.. The 510(k) number is K153160.
When did AVIVO Mobile Patient Management (MPM) System receive FDA 510(k) clearance?
AVIVO Mobile Patient Management (MPM) System received FDA 510(k) clearance on 2016-03-30, under 510(k) number K153160.
Who is the listed applicant for AVIVO Mobile Patient Management (MPM) System?
The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medtronic, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MHX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.