K-number	K141795
Device name	BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500
Applicant	R & D Batteries, Inc.
Product code	MKJ
Device class	Class III
Decision date	Dec 8, 2014
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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BATTER PACK, REPLACEMENT FOR PHYSIO CONTROL LIFEPAK 500

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