Babylog VN800, Babylog VN600
K 號：K222207 · 2023-05-16
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器材摘要
Babylog VN800, Babylog VN600 is the device name listed in this FDA 510(k) record. The listed applicant is Draegerwerk AG & CO Kgaa. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K222207. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Babylog VN800, Babylog VN600?
Babylog VN800, Babylog VN600 is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Draegerwerk AG & CO Kgaa. The 510(k) number is K222207.
When did Babylog VN800, Babylog VN600 receive FDA 510(k) clearance?
Babylog VN800, Babylog VN600 received FDA 510(k) clearance on 2023-05-16, under 510(k) number K222207.
Who is the listed applicant for Babylog VN800, Babylog VN600?
The FDA 510(k) record lists Draegerwerk AG & CO Kgaa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Babylog VN800, Babylog VN600?
The FDA product code for Babylog VN800, Babylog VN600 is CBK.
相關臨床試驗
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其他以 Draegerwerk AG & CO Kgaa 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：CBK）
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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