HippoMind (v1.0)
K 號：K251881 · 2025-12-03
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器材摘要
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.
常見問題
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.
相關臨床試驗
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相關器械（代碼：OLT）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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