Express SD Biliary Monorail Premounted Stent System
K号: K162404 · 2016-10-12
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器械摘要
常见问题
What is the Express SD Biliary Monorail Premounted Stent System?
Express SD Biliary Monorail Premounted Stent System is a medical device that received FDA 510(k) clearance on 2016-10-12. The listed applicant is Boston Scientific Corporation. The 510(k) number is K162404.
When did Express SD Biliary Monorail Premounted Stent System receive FDA 510(k) clearance?
Express SD Biliary Monorail Premounted Stent System received FDA 510(k) clearance on 2016-10-12, under 510(k) number K162404.
Who is the listed applicant for Express SD Biliary Monorail Premounted Stent System?
The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Express SD Biliary Monorail Premounted Stent System?
The FDA product code for Express SD Biliary Monorail Premounted Stent System is FGE.
相关临床试验
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列明Boston Scientific Corporation为申报人的其他记录
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相关器械（代码：FGE）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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