K-number	K010083
Device name	TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT, MODEL 466-P306A
Applicant	Cordis Corp.
Product code	DTK
Device class	Class II
Decision date	Jun 6, 2001
Decision	Substantially Equivalent
Regulation	870.3375

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View the full FDA submission: accessdata.fda.gov

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TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT, MODEL 466-P306A

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