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FDA 510(k)

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT

K-Number: K000062 · 2000-07-07

ApplicantCordis Corp.
Decision Date2000-07-07
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 2000-07-07 under 510(k) number K000062. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT?

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT is a medical device that received FDA 510(k) clearance on 2000-07-07. The listed applicant is Cordis Corp.. The 510(k) number is K000062.

When did CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT receive FDA 510(k) clearance?

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT received FDA 510(k) clearance on 2000-07-07, under 510(k) number K000062.

Who is the listed applicant for CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT?

The FDA 510(k) record lists Cordis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT?

The FDA product code for CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT is DTK.

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Related Devices (Code: DTK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K242612Option ELITE Vena Cava Filter System (352506070E 352506100E)Argon Medical Devices, Inc.K240578VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter SystemB.Braun Medical, Inc.K241507ALN Optional Vena Cava Filter (FB.010500, FF.010995, FJ.120096, FB.HOOK, FF.HOOK, FJ.HOOK)Aln S.A.R.L.K240257Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery KitBdK233680Celect Platinum Vena Cava Filter Set for Femoral Vein Approach (IGTCFS-65-1-FEM-CELECT-PT); Celect Platinum Vena Cava Filter Set for Jugular Vein Approach (IGTCFS-65-1-JUG-CELECT-PT); Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach (IGTCFS-65-1-UNI-CELECT-PT); Günther Tulip Vena Cava Filter Set for Femoral Vein Approach (IGTCFS-65-1-FEM-TULIP); Günther Tulip Vena Cava Filter Set for Jugular Vein Approach (IGTCFS-65-1-JUG-TULIP); Günther Tulip Vena Cava FilterWilliam Cook Europe ApsK211874Günther Tulip Vena Cava Filter Set for Femoral Vein Approach, Günther Tulip Vena Cava Filter Set for Jugular Vein Approach, Günther Tulip Vena Cava Filter Set for Femoral and Jugular Vein ApproachWilliam Cook Europe Aps

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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