K-number	K130454
Device name	LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR
Applicant	Physio-Control, Inc.
Product code	MKJ
Device class	Class III
Decision date	Aug 21, 2013
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR

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