K-number	K062233
Device name	HEARTSTART MRX MONITOR/DEFIBRILLATOR
Applicant	Philips Medical Systems North America, Inc.
Product code	MKJ
Device class	Class III
Decision date	Nov 22, 2006
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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HEARTSTART MRX MONITOR/DEFIBRILLATOR

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