內血管輸注設備組合,含閥門和分配器
K 號:K223175 · 2023-03-10
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器材摘要
常見問題
What is the lntravascular Administration Sets with Stopcock and Manifold?
lntravascular Administration Sets with Stopcock and Manifold is a medical device that received FDA 510(k) clearance on 2023-03-10. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K223175.
When did lntravascular Administration Sets with Stopcock and Manifold receive FDA 510(k) clearance?
lntravascular Administration Sets with Stopcock and Manifold received FDA 510(k) clearance on 2023-03-10, under 510(k) number K223175.
Who is the listed applicant for lntravascular Administration Sets with Stopcock and Manifold?
The FDA 510(k) record lists Baxter Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for lntravascular Administration Sets with Stopcock and Manifold?
The FDA product code for lntravascular Administration Sets with Stopcock and Manifold is FMG.
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 Baxter Healthcare 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:FMG)
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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