K-number	K072923
Device name	ZOLL E SERIES DEFIBRILLATOR
Applicant	Zoll Medical Corporation, World Wide Headquarters
Product code	MKJ
Device class	Class III
Decision date	Apr 24, 2008
Decision	Substantially Equivalent
Regulation	870.5310

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Source

View the full FDA submission: accessdata.fda.gov

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ZOLL E SERIES DEFIBRILLATOR

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