K-number	K021547
Device name	FLOWLINE BIOPORE EPTFE VASCULAR GRAFT
Applicant	Jotec GmbH
Product code	DSY
Device class	Class II
Decision date	Jan 24, 2003
Decision	Substantially Equivalent
Regulation	870.3450

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View the full FDA submission: accessdata.fda.gov

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FLOWLINE BIOPORE EPTFE VASCULAR GRAFT

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