GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER
K-Number: K090140 · 2009-04-03
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Device Summary
Frequently Asked Questions
What is the GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER?
GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER is a medical device that received FDA 510(k) clearance on 2009-04-03. The listed applicant is William Cook Europe Aps. The 510(k) number is K090140.
When did GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER receive FDA 510(k) clearance?
GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER received FDA 510(k) clearance on 2009-04-03, under 510(k) number K090140.
Who is the listed applicant for GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER?
The FDA 510(k) record lists William Cook Europe Aps as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GUNTHER TULIP VENA CAVA FILTER, COOK CELECT VENA CAVA FILTER?
The FDA product code for GUNTHER TULIP VENA CAVA FILTER, COOK CELECT 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 William Cook Europe Aps 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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