EXPANDABLE BILIARY STENT ENDOPROSTHESIS
K-Number: K885180 · 1989-02-16
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Device Summary
Frequently Asked Questions
What is the EXPANDABLE BILIARY STENT ENDOPROSTHESIS?
EXPANDABLE BILIARY STENT ENDOPROSTHESIS is a medical device that received FDA 510(k) clearance on 1989-02-16. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K885180.
When did EXPANDABLE BILIARY STENT ENDOPROSTHESIS receive FDA 510(k) clearance?
EXPANDABLE BILIARY STENT ENDOPROSTHESIS received FDA 510(k) clearance on 1989-02-16, under 510(k) number K885180.
Who is the listed applicant for EXPANDABLE BILIARY STENT ENDOPROSTHESIS?
The FDA 510(k) record lists Schneider Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXPANDABLE BILIARY STENT ENDOPROSTHESIS?
The FDA product code for EXPANDABLE BILIARY STENT ENDOPROSTHESIS 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 Schneider Intl., Ltd. 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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