K-number	K072527
Device name	AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
Applicant	Zoll Circulation
Product code	DRM
Device class	Class II
Decision date	Mar 19, 2008
Decision	Substantially Equivalent
Regulation	870.5200

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View the full FDA submission: accessdata.fda.gov

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AUTOPULSE RESUSCITATION SYSTEM, MODEL 100

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