FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

HEARSTART MRX WITH AIRWAY CONFIMRATION ASSIST

K Number: K130153 · Decision Mar 12, 2013
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
227
Applicant Total
97
Review Days
49

Basic Information

Device Name
HEARSTART MRX WITH AIRWAY CONFIMRATION ASSIST
K Number
K130153
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS
Date Received
January 22, 2013
Decision Date
March 12, 2013
Product Code
MKJ
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
MKJ Automated External Defibrillators (Non-Wearable)

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K142935 CareEvent
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