K-number	K983393
Device name	LIFEPAK 500 BIPHASIC
Applicant	Physio-Control Corp.
Product code	MKJ
Device class	Class III
Decision date	May 5, 1999
Decision	Substantially Equivalent - Subject to Tracking Reg.
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 500 BIPHASIC

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