SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO.
K-Number: K896163 · 1989-12-01
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Device Summary
Frequently Asked Questions
What is the SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO.?
SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO. is a medical device that received FDA 510(k) clearance on 1989-12-01. The listed applicant is Schneider Stent. The 510(k) number is K896163.
When did SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO. receive FDA 510(k) clearance?
SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO. received FDA 510(k) clearance on 1989-12-01, under 510(k) number K896163.
Who is the listed applicant for SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO.?
The FDA 510(k) record lists Schneider Stent as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO.?
The FDA product code for SCHNEIDER STENT WALLSTENT ENDOSCOPIC BILIARY ENDO. 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.
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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