K-number	K013944
Device name	JOSTRA DUAL STAGE VENOUS RETURN CANNULAE
Applicant	Jostra AG
Product code	DWF
Device class	Class II
Decision date	Feb 11, 2002
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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JOSTRA DUAL STAGE VENOUS RETURN CANNULAE

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