K-number	K080034
Device name	THREE STAGE VENOUS RETURN CANNULA, MODEL 816460
Applicant	Terumo Cardiovascular Systems Corp.
Product code	DWF
Device class	Class II
Decision date	Jun 17, 2008
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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THREE STAGE VENOUS RETURN CANNULA, MODEL 816460

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