DURAMAX .018 BILIARY STENT SYSTEM
K-Number: K032436 · 2004-02-04
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Device Summary
Frequently Asked Questions
What is the DURAMAX .018 BILIARY STENT SYSTEM?
DURAMAX .018 BILIARY STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2004-02-04. The listed applicant is Avantec Vascular Corp.. The 510(k) number is K032436.
When did DURAMAX .018 BILIARY STENT SYSTEM receive FDA 510(k) clearance?
DURAMAX .018 BILIARY STENT SYSTEM received FDA 510(k) clearance on 2004-02-04, under 510(k) number K032436.
Who is the listed applicant for DURAMAX .018 BILIARY STENT SYSTEM?
The FDA 510(k) record lists Avantec Vascular Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DURAMAX .018 BILIARY STENT SYSTEM?
The FDA product code for DURAMAX .018 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 Avantec Vascular Corp. 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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