K-number	K052057
Device name	LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
Applicant	Medtronic Emergency Response Systems, Inc.
Product code	MKJ
Device class	Class III
Decision date	Feb 17, 2006
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

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