HippoMind (v1.0)
K号: K251881 · 2025-12-03
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申请人Hippoclinic
决定日期2025-12-03
产品代码OLT
咨询委员会NE
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决定实质等同
器械摘要
HippoMind (v1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Hippoclinic. It received FDA 510(k) clearance on 2025-12-03 under 510(k) number K251881. The device is classified under product code OLT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the HippoMind (v1.0)?
HippoMind (v1.0) is a medical device that received FDA 510(k) clearance on 2025-12-03. The listed applicant is Hippoclinic. The 510(k) number is K251881.
When did HippoMind (v1.0) receive FDA 510(k) clearance?
HippoMind (v1.0) received FDA 510(k) clearance on 2025-12-03, under 510(k) number K251881.
Who is the listed applicant for HippoMind (v1.0)?
The FDA 510(k) record lists Hippoclinic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HippoMind (v1.0)?
The FDA product code for HippoMind (v1.0) is OLT.
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。
相关器械（代码：OLT）
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。
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官方来源
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