K-number	K902478
Device name	LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR
Applicant	Physio-Control Corp.
Product code	LDD
Device class	Class II
Decision date	Oct 31, 1990
Decision	Substantially Equivalent
Regulation	870.5300

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR

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