K-number	K040173
Device name	PEDIATRIC AORTIC ROOT CANNULA
Applicant	Medtronic Perfusion Systems
Product code	DWF
Device class	Class II
Decision date	Mar 19, 2004
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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PEDIATRIC AORTIC ROOT CANNULA

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