K-number	K092509
Device name	EDWARDS LIFESCIENCES VENOUS RETURN CANNULAE
Applicant	Edwards Lifesciences, LLC
Product code	DWF
Device class	Class II
Decision date	Oct 8, 2009
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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EDWARDS LIFESCIENCES VENOUS RETURN CANNULAE

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