Access anti-HAV
K 號:K243846 · 2025-09-09
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器材摘要
Access anti-HAV is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Coulter, Inc.. It received FDA 510(k) clearance on 2025-09-09 under 510(k) number K243846. The device is classified under product code LOL. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Access anti-HAV?
Access anti-HAV is a medical device that received FDA 510(k) clearance on 2025-09-09. The listed applicant is Beckman Coulter, Inc.. The 510(k) number is K243846.
When did Access anti-HAV receive FDA 510(k) clearance?
Access anti-HAV received FDA 510(k) clearance on 2025-09-09, under 510(k) number K243846.
Who is the listed applicant for Access anti-HAV?
FDA 510(k) 記錄將 Beckman Coulter, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Access anti-HAV?
The FDA product code for Access anti-HAV is LOL.
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 Beckman Coulter, Inc. 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:LOL)
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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