K-number	K040637
Device name	POWERHEART AED G3 PRO
Applicant	Cardiac Science, Inc.
Product code	MKJ
Device class	Class III
Decision date	Aug 6, 2004
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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POWERHEART AED G3 PRO

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