單次使用細胞學刷V型（BC-V600P-3010）
K 號：K250993 · 2025-12-18
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器材摘要
Single Use Cytology Brush V (BC-V600P-3010) is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2025-12-18 under 510(k) number K250993. The device is classified under product code FDX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Single Use Cytology Brush V (BC-V600P-3010)?
Single Use Cytology Brush V (BC-V600P-3010) is a medical device that received FDA 510(k) clearance on 2025-12-18. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K250993.
When did Single Use Cytology Brush V (BC-V600P-3010) receive FDA 510(k) clearance?
Single Use Cytology Brush V (BC-V600P-3010) received FDA 510(k) clearance on 2025-12-18, under 510(k) number K250993.
Who is the listed applicant for Single Use Cytology Brush V (BC-V600P-3010)?
FDA 510(k) 記錄中將Olympus Medical Systems Corporation列為申請人。這並不單獨確立該設備製造商。
What is the FDA product code for Single Use Cytology Brush V (BC-V600P-3010)?
The FDA product code for Single Use Cytology Brush V (BC-V600P-3010) is FDX.
相關臨床試驗
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。
其他以 Olympus Medical Systems Corporation 為申請人之記錄
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。
相關器械（代碼：FDX）
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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