K-number	K103567
Device name	LIFEPAK 15 MONITOR/DEFIBRILLATOR
Applicant	Physio-Control, Inc.
Product code	MKJ
Device class	Class III
Decision date	Mar 22, 2011
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 15 MONITOR/DEFIBRILLATOR

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