K-number	K063510
Device name	LIFEPAK 12 DEFIBRILLATOR/MONITOR
Applicant	Medtronic Emergency Response Systems, Inc.
Product code	MKJ
Device class	Class III
Decision date	Jan 26, 2007
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 12 DEFIBRILLATOR/MONITOR

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