K-number	K853564
Device name	LIFEPAK 200
Applicant	Physio-Control Corp.
Product code	MKJ
Device class	Class III
Decision date	Oct 11, 1985
Decision	Substantially Equivalent
Regulation	870.5310

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 200

Everything you need for a 510(k) submission. Nothing you don't.