PHILIPS M5066A AND M5068A

Automated External Defibrillators (non-wearable)

PHILIPS MEDICAL SYSTEMS

The following data is part of a premarket notification filed by Philips Medical Systems with the FDA for Philips M5066a And M5068a.

Pre-market Notification Details

Device IDK020715
510k NumberK020715
Device Name:PHILIPS M5066A AND M5068A
ClassificationAutomated External Defibrillators (non-wearable)
Applicant PHILIPS MEDICAL SYSTEMS 2301 FIFTH AVE., SUITE 200 Seattle,  WA  98121
ContactTamara Yount
CorrespondentTamara Yount
PHILIPS MEDICAL SYSTEMS 2301 FIFTH AVE., SUITE 200 Seattle,  WA  98121
Product CodeMKJ  
CFR Regulation Number870.5310 [🔎]
DecisionSe Subject To Tracking Reg (ST)
TypeAbbreviated
3rd Party ReviewedNo
Combination ProductNo
Date Received2002-03-05
Decision Date2002-11-08
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00884838075849 K020715 000
00884838051478 K020715 000
00884838050686 K020715 000
00884838050679 K020715 000
00884838049123 K020715 000
00884838023840 K020715 000
00884838023758 K020715 000
00884838023741 K020715 000

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