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FDA 510(k), K003964, TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND 466-P306B
FDA 510(k), K003964, TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND 466-P306B
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510(K) Number: K003964
Device Name: TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND 466-P306B
Manufacturer: CORDIS CORP.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 12/22/2000
Decision Date: 01/19/2001
Regulation Medical Specialty: Cardiovascular
Device Name: TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND 466-P306B
Manufacturer: CORDIS CORP.
Device Classification Name: filter, intravascular, cardiovascular
Regulation Number: 870.3375
Classification Product Code: DTK
Date Received: 12/22/2000
Decision Date: 01/19/2001
Regulation Medical Specialty: Cardiovascular
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