Alivio 室内导管和冲洗系统(Alivio 系统)
K号: K172006 · 2017-11-09
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器械摘要
常见问题
What is the Alivio Ventricular Catheter and Flusher System (Alivio System)?
Alivio Ventricular Catheter and Flusher System (Alivio System) is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Alcyone Lifesciences, Inc.. The 510(k) number is K172006.
When did Alivio Ventricular Catheter and Flusher System (Alivio System) receive FDA 510(k) clearance?
Alivio Ventricular Catheter and Flusher System (Alivio System) received FDA 510(k) clearance on 2017-11-09, under 510(k) number K172006.
Who is the listed applicant for Alivio Ventricular Catheter and Flusher System (Alivio System)?
The FDA 510(k) record lists Alcyone Lifesciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alivio Ventricular Catheter and Flusher System (Alivio System)?
The FDA product code for Alivio Ventricular Catheter and Flusher System (Alivio System) is JXG.
相关临床试验
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相关器械(代码:JXG)
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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