WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM
K-Number: K031331 · 2003-08-12
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Device Summary
Frequently Asked Questions
What is the WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM?
WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM is a medical device that received FDA 510(k) clearance on 2003-08-12. The listed applicant is Abbott Vascular, Inc.. The 510(k) number is K031331.
When did WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM receive FDA 510(k) clearance?
WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM received FDA 510(k) clearance on 2003-08-12, under 510(k) number K031331.
Who is the listed applicant for WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM?
The FDA 510(k) record lists Abbott Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM?
The FDA product code for WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY 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 Abbott Vascular, 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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