LUMINEXX ENDOSCOPIC BILIARY STENT
K-Number: K031186 · 2003-05-06
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Device Summary
Frequently Asked Questions
What is the LUMINEXX ENDOSCOPIC BILIARY STENT?
LUMINEXX ENDOSCOPIC BILIARY STENT is a medical device that received FDA 510(k) clearance on 2003-05-06. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K031186.
When did LUMINEXX ENDOSCOPIC BILIARY STENT receive FDA 510(k) clearance?
LUMINEXX ENDOSCOPIC BILIARY STENT received FDA 510(k) clearance on 2003-05-06, under 510(k) number K031186.
Who is the listed applicant for LUMINEXX ENDOSCOPIC BILIARY STENT?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUMINEXX ENDOSCOPIC BILIARY STENT?
The FDA product code for LUMINEXX ENDOSCOPIC 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 C.R. Bard, 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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