K-number	K072172
Device name	JOSTRA PEDIATRIC ARTERIAL PREFUSION CANNULAE
Applicant	Maquet Cardiopulmonary, AG
Product code	DWF
Device class	Class II
Decision date	Aug 31, 2007
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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JOSTRA PEDIATRIC ARTERIAL PREFUSION CANNULAE

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