K-number	K935674
Device name	LIFEPAK 9 DEFIBRILLATOR/MONITOR
Applicant	Physio-Control Corp.
Product code	LDD
Device class	Class II
Decision date	Dec 16, 1993
Decision	Substantially Equivalent
Regulation	870.5300

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View the full FDA submission: accessdata.fda.gov

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LIFEPAK 9 DEFIBRILLATOR/MONITOR

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