K-number	K043179
Device name	SELECT 3D ARTERIAL CANNULA
Applicant	Medtronic Perfusion Systems
Product code	DWF
Device class	Class II
Decision date	Feb 8, 2005
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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SELECT 3D ARTERIAL CANNULA

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