K-number	K033275
Device name	LIFEPAK 12, 20, 500, CR PLUS
Applicant	Medtronic Physio-Control Corp.
Product code	MKJ
Device class	Class III
Decision date	Nov 6, 2003
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 12, 20, 500, CR PLUS

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