DeepBT Detector-Plus
K 號：K252190 · 2026-04-10
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器材摘要
DeepBT Detector-Plus is the device name listed in this FDA 510(k) record. The listed applicant is Aitewan Biomedical Technology, Inc.. It received FDA 510(k) clearance on 2026-04-10 under 510(k) number K252190. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DeepBT Detector-Plus?
DeepBT Detector-Plus is a medical device that received FDA 510(k) clearance on 2026-04-10. The listed applicant is Aitewan Biomedical Technology, Inc.. The 510(k) number is K252190.
When did DeepBT Detector-Plus receive FDA 510(k) clearance?
DeepBT Detector-Plus received FDA 510(k) clearance on 2026-04-10, under 510(k) number K252190.
Who is the listed applicant for DeepBT Detector-Plus?
The FDA 510(k) record lists Aitewan Biomedical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DeepBT Detector-Plus?
The FDA product code for DeepBT Detector-Plus is QKB.
相關臨床試驗
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相關器械（代碼：QKB）
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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