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

M3290A INTELLIVUE INFORMATION CENTER SOFTWARE, RELEASE 1.00

K Number: K081983 · Decision Aug 22, 2008
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
411
Applicant Total
97
Review Days
42

Basic Information

Device Name
M3290A INTELLIVUE INFORMATION CENTER SOFTWARE, RELEASE 1.00
K Number
K081983
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS
Date Received
July 11, 2008
Decision Date
August 22, 2008
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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K133659 HEARTSTART XL+DEFIBRILLATOR/MONITOR WITH END-TIDAL CARBON DIOXIDE MONITORING
K142935 CareEvent
K143057 M3290B Philips IntelliVue Information Center iX
K133603 PHILIPS CT DYNAMIC MYOCARDIAL PERFUSION (DMP) APPLICATION
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