PeekMed web
K号: K251096 · 2025-07-14
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器械摘要
PeekMed web is the device name listed in this FDA 510(k) record. The listed applicant is Peek Health, S.A.. It received FDA 510(k) clearance on 2025-07-14 under 510(k) number K251096. 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 PeekMed web?
PeekMed web is a medical device that received FDA 510(k) clearance on 2025-07-14. The listed applicant is Peek Health, S.A.. The 510(k) number is K251096.
When did PeekMed web receive FDA 510(k) clearance?
PeekMed web received FDA 510(k) clearance on 2025-07-14, under 510(k) number K251096.
Who is the listed applicant for PeekMed web?
The FDA 510(k) record lists Peek Health, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PeekMed web?
The FDA product code for PeekMed web is QIH.
相关临床试验
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列明Peek Health, S.A.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：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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