NIROYAL BILIARY PREMOUNTED STENT SYSTEM
K-Number: K003929 · 2001-03-22
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Device Summary
Frequently Asked Questions
What is the NIROYAL BILIARY PREMOUNTED STENT SYSTEM?
NIROYAL BILIARY PREMOUNTED STENT SYSTEM is a medical device that received FDA 510(k) clearance on 2001-03-22. The listed applicant is Boston Scientific Corp. The 510(k) number is K003929.
When did NIROYAL BILIARY PREMOUNTED STENT SYSTEM receive FDA 510(k) clearance?
NIROYAL BILIARY PREMOUNTED STENT SYSTEM received FDA 510(k) clearance on 2001-03-22, under 510(k) number K003929.
Who is the listed applicant for NIROYAL BILIARY PREMOUNTED STENT SYSTEM?
The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIROYAL BILIARY PREMOUNTED STENT SYSTEM?
The FDA product code for NIROYAL BILIARY PREMOUNTED 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 Boston Scientific 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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