FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AVIVO Mobile Patient Management (MPM) System

K Number: K153160 · Decision Mar 30, 2016
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
25
Review Days
149

Basic Information

Device Name
AVIVO Mobile Patient Management (MPM) System
K Number
K153160
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC, INC.
Date Received
November 2, 2015
Decision Date
March 30, 2016
Product Code
MHX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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