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FDA 510(k)

GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET

K-Number: K032426 · 2003-10-31

ApplicantCook, Inc.
Decision Date2003-10-31
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 2003-10-31 under 510(k) number K032426. 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 GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET?

GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET is a medical device that received FDA 510(k) clearance on 2003-10-31. The listed applicant is Cook, Inc.. The 510(k) number is K032426.

When did GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET receive FDA 510(k) clearance?

GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET received FDA 510(k) clearance on 2003-10-31, under 510(k) number K032426.

Who is the listed applicant for GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET?

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

What is the FDA product code for GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET?

The FDA product code for GUNHTER TULIP VENA CAVA MREYE FILTER AND RETRIEVAL SET is DTK.

Related Clinical Trials

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.

Other records listing Cook, Inc. as applicant

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.

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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.

Official Source

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

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