Nooro身体和足部刺激器(SM9141,SM9142)
K号: K243334 · 2024-11-22
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器械摘要
常见问题
What is the Nooro Body & Foot Stimulator (SM9141, SM9142)?
Nooro Body & Foot Stimulator (SM9141, SM9142) is a medical device that received FDA 510(k) clearance on 2024-11-22. The listed applicant is Xf Agencija Limited. The 510(k) number is K243334.
When did Nooro Body & Foot Stimulator (SM9141, SM9142) receive FDA 510(k) clearance?
Nooro Body & Foot Stimulator (SM9141, SM9142) received FDA 510(k) clearance on 2024-11-22, under 510(k) number K243334.
Who is the listed applicant for Nooro Body & Foot Stimulator (SM9141, SM9142)?
The FDA 510(k) record lists Xf Agencija Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nooro Body & Foot Stimulator (SM9141, SM9142)?
The FDA product code for Nooro Body & Foot Stimulator (SM9141, SM9142) is NUH.
相关临床试验
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相关器械(代码:NUH)
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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