GUNTHER TULIP VENA CAVA FILTER
K-Number: K072240 · 2007-11-08
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Device Summary
Frequently Asked Questions
What is the GUNTHER TULIP VENA CAVA FILTER?
GUNTHER TULIP VENA CAVA FILTER is a medical device that received FDA 510(k) clearance on 2007-11-08. The listed applicant is Cook, Inc.. The 510(k) number is K072240.
When did GUNTHER TULIP VENA CAVA FILTER receive FDA 510(k) clearance?
GUNTHER TULIP VENA CAVA FILTER received FDA 510(k) clearance on 2007-11-08, under 510(k) number K072240.
Who is the listed applicant for GUNTHER TULIP VENA CAVA FILTER?
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 GUNTHER TULIP VENA CAVA FILTER?
The FDA product code for GUNTHER TULIP VENA CAVA FILTER 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.
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
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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