PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90

Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)

PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH

The following data is part of a premarket notification filed by Philips Medizinsysteme Boeblingen Gmbh with the FDA for Philips Intellivue Patient Monitor, Models Mp20, Mp30, Mp40, Mp50, Mp60, Mp70 And Mp90.

Pre-market Notification Details

Device IDK050762
510k NumberK050762
Device Name:PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP20, MP30, MP40, MP50, MP60, MP70 AND MP90
ClassificationMonitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
Applicant PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, Baden-wttbg,  DE D-71034
ContactEgon Pfeil
CorrespondentEgon Pfeil
PHILIPS MEDIZINSYSTEME BOEBLINGEN GMBH HEWLETT-PACKARD STR.2 Boeblingen, Baden-wttbg,  DE D-71034
Product CodeMHX  
CFR Regulation Number870.1025 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2005-03-24
Decision Date2005-04-22
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00884838072169 K050762 000
00884838072152 K050762 000
00884838072145 K050762 000
00884838021549 K050762 000
20884838072187 K050762 000
20884838072170 K050762 000

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