Relu 云
K号: K252708 · 2026-04-10
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器械摘要
Relu Cloud is the device name listed in this FDA 510(k) record. The listed applicant is Relu BV. It received FDA 510(k) clearance on 2026-04-10 under 510(k) number K252708. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Relu Cloud?
Relu Cloud is a medical device that received FDA 510(k) clearance on 2026-04-10. The listed applicant is Relu BV. The 510(k) number is K252708.
When did Relu Cloud receive FDA 510(k) clearance?
Relu Cloud received FDA 510(k) clearance on 2026-04-10, under 510(k) number K252708.
Who is the listed applicant for Relu Cloud?
The FDA 510(k) record lists Relu BV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Relu Cloud?
The FDA product code for Relu Cloud is QIH.
相关临床试验
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列明Relu BV为申报人的其他记录
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相关器械（代码：QIH）
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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