K-number	K112998
Device name	AUTOPULSE RESUSCITATION SYSTEM MODEL 1000
Applicant	Zoll Circulation
Product code	DRM
Device class	Class II
Decision date	Mar 15, 2012
Decision	Substantially Equivalent
Regulation	870.5200

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Source

View the full FDA submission: accessdata.fda.gov

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AUTOPULSE RESUSCITATION SYSTEM MODEL 1000

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