K-number	K060559
Device name	ZOLL R SERIES DEFIBRILLATOR
Applicant	ZOLL Medical Corporation
Product code	MKJ
Device class	Class III
Decision date	Aug 17, 2006
Decision	Substantially Equivalent
Regulation	870.5310

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Source

View the full FDA submission: accessdata.fda.gov

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ZOLL R SERIES DEFIBRILLATOR

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