Nunchaku
K号: K161373 · 2016-11-03
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器械摘要
Nunchaku is the device name listed in this FDA 510(k) record. The listed applicant is Fci (France Chirurgie Instrumentation). It received FDA 510(k) clearance on 2016-11-03 under 510(k) number K161373. The device is classified under product code OKS. FDA Decision: Substantially Equivalent.
常见问题
What is the Nunchaku?
Nunchaku is a medical device that received FDA 510(k) clearance on 2016-11-03. The listed applicant is Fci (France Chirurgie Instrumentation). The 510(k) number is K161373.
When did Nunchaku receive FDA 510(k) clearance?
Nunchaku received FDA 510(k) clearance on 2016-11-03, under 510(k) number K161373.
Who is the listed applicant for Nunchaku?
The FDA 510(k) record lists Fci (France Chirurgie Instrumentation) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nunchaku?
The FDA product code for Nunchaku is OKS.
相关临床试验
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相关器械（代码：OKS）
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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