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K 號：K240312 · 2024-08-01
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器材摘要
Infinity CentralStation Wide is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-08-01 under 510(k) number K240312. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Infinity CentralStation Wide?
Infinity CentralStation Wide is a medical device that received FDA 510(k) clearance on 2024-08-01. The listed applicant is Draeger Medical Systems, Inc.. The 510(k) number is K240312.
When did Infinity CentralStation Wide receive FDA 510(k) clearance?
Infinity CentralStation Wide received FDA 510(k) clearance on 2024-08-01, under 510(k) number K240312.
Who is the listed applicant for Infinity CentralStation Wide?
FDA 510(k) 記錄將 Draeger Medical Systems, 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 Infinity CentralStation Wide?
The FDA product code for Infinity CentralStation Wide is MHX.
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 Draeger Medical Systems, 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：MHX）
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。
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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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