K-number	K063119
Device name	LIFEPAK 20 DEFIBRILLATOR/ MONITOR
Applicant	Medtronic Emergency Response Systems, Inc.
Product code	MKJ
Device class	Class III
Decision date	Dec 22, 2006
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

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