EVOLUTION BILIARY STENT SYSTEM
K-Number: K121430 · 2013-03-01
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Device Summary
Frequently Asked Questions
What is the EVOLUTION BILIARY STENT SYSTEM?
EVOLUTION BILIARY STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2013-03-01. The listed applicant is Cook Ireland, Ltd.. The 510(k) number is K121430.
When did EVOLUTION BILIARY STENT SYSTEM receive FDA 510(k) clearance?
EVOLUTION BILIARY STENT SYSTEM received FDA 510(k) clearance on 2013-03-01, under 510(k) number K121430.
Who is the listed applicant for EVOLUTION BILIARY STENT SYSTEM?
The FDA 510(k) record lists Cook Ireland, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVOLUTION BILIARY STENT SYSTEM?
The FDA product code for EVOLUTION BILIARY STENT SYSTEM 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 Ireland, Ltd. 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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