Scaida 腦部CT-ICH (v1.0)
K 號：K250694 · 2025-11-25
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器材摘要
Scaida BrainCT-ICH (v1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Mlhealth 360. It received FDA 510(k) clearance on 2025-11-25 under 510(k) number K250694. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Scaida BrainCT-ICH (v1.0)?
Scaida BrainCT-ICH (v1.0) is a medical device that received FDA 510(k) clearance on 2025-11-25. The listed applicant is Mlhealth 360. The 510(k) number is K250694.
When did Scaida BrainCT-ICH (v1.0) receive FDA 510(k) clearance?
Scaida BrainCT-ICH (v1.0) received FDA 510(k) clearance on 2025-11-25, under 510(k) number K250694.
Who is the listed applicant for Scaida BrainCT-ICH (v1.0)?
The FDA 510(k) record lists Mlhealth 360 as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scaida BrainCT-ICH (v1.0)?
The FDA product code for Scaida BrainCT-ICH (v1.0) is QAS.
相關臨床試驗
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相關器械（代碼：QAS）
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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