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FDA 510(k)

Günther Tulip® Vena Cava Filter Retrieval Set

K-Number: K181757 · 2018-11-06

ApplicantCook Incorporated
Decision Date2018-11-06
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Günther Tulip® Vena Cava Filter Retrieval Set is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2018-11-06 under approval number K181757. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Günther Tulip® Vena Cava Filter Retrieval Set?

Günther Tulip® Vena Cava Filter Retrieval Set is a medical device that received FDA 510(k) clearance on 2018-11-06. It is manufactured by Cook Incorporated. The 510(k) number is K181757.

When was Günther Tulip® Vena Cava Filter Retrieval Set approved by the FDA?

Günther Tulip® Vena Cava Filter Retrieval Set received FDA 510(k) clearance on 2018-11-06, under approval number K181757.

What company makes Günther Tulip® Vena Cava Filter Retrieval Set?

Günther Tulip® Vena Cava Filter Retrieval Set is manufactured by Cook Incorporated.

What is the FDA product code for Günther Tulip® Vena Cava Filter Retrieval Set?

The FDA product code for Günther Tulip® Vena Cava Filter Retrieval Set is MMX.

Related Clinical Trials

NCT05881798 Post-Market Celect Platinum Vena Cava Filter and Gunther Tulip Retrieval Set Study RECRUITING

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Related Devices (Code: MMX)

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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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