Fiagon 导航 - PointerTube 直线和 PointerTube Keat
K号: K163416 · 2017-02-16
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器械摘要
常见问题
What is the Fiagon Navigation – PointerTube Straight and PointerTube Keat?
Fiagon Navigation – PointerTube Straight and PointerTube Keat is a medical device that received FDA 510(k) clearance on 2017-02-16. The listed applicant is Fiagon GmbH. The 510(k) number is K163416.
When did Fiagon Navigation – PointerTube Straight and PointerTube Keat receive FDA 510(k) clearance?
Fiagon Navigation – PointerTube Straight and PointerTube Keat received FDA 510(k) clearance on 2017-02-16, under 510(k) number K163416.
Who is the listed applicant for Fiagon Navigation – PointerTube Straight and PointerTube Keat?
The FDA 510(k) record lists Fiagon GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fiagon Navigation – PointerTube Straight and PointerTube Keat?
The FDA product code for Fiagon Navigation – PointerTube Straight and PointerTube Keat is PGW.
相关临床试验
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列明Fiagon GmbH为申报人的其他记录
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。
相关器械(代码:PGW)
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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