PointerShell 通用型,PointerShell LS
K号: K160479 · 2016-03-23
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器械摘要
常见问题
What is the PointerShell Universal, PointerShell LS?
PointerShell Universal, PointerShell LS is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Fiagon GmbH. The 510(k) number is K160479.
When did PointerShell Universal, PointerShell LS receive FDA 510(k) clearance?
PointerShell Universal, PointerShell LS received FDA 510(k) clearance on 2016-03-23, under 510(k) number K160479.
Who is the listed applicant for PointerShell Universal, PointerShell LS?
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 PointerShell Universal, PointerShell LS?
The FDA product code for PointerShell Universal, PointerShell LS is PGW.
相关临床试验
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。
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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