COOK ZILVER BILIARY STENT
K-Number: K010242 · 2001-08-13
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Device Summary
Frequently Asked Questions
What is the COOK ZILVER BILIARY STENT?
COOK ZILVER BILIARY STENT is a medical device that received FDA 510(k) clearance on 2001-08-13. The listed applicant is Cook, Inc.. The 510(k) number is K010242.
When did COOK ZILVER BILIARY STENT receive FDA 510(k) clearance?
COOK ZILVER BILIARY STENT received FDA 510(k) clearance on 2001-08-13, under 510(k) number K010242.
Who is the listed applicant for COOK ZILVER BILIARY STENT?
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 COOK ZILVER BILIARY STENT?
The FDA product code for COOK ZILVER BILIARY STENT is FGE.
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: FGE)
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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