守衛網智能解釋器
K 號：K153654 · 2016-09-16
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器材摘要
Sentry WEB SmartInterp is the device name listed in this FDA 510(k) record. The listed applicant is Carefusion Germany 234 GmbH. It received FDA 510(k) clearance on 2016-09-16 under 510(k) number K153654. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Sentry WEB SmartInterp?
Sentry WEB SmartInterp is a medical device that received FDA 510(k) clearance on 2016-09-16. The listed applicant is Carefusion Germany 234 GmbH. The 510(k) number is K153654.
When did Sentry WEB SmartInterp receive FDA 510(k) clearance?
Sentry WEB SmartInterp received FDA 510(k) clearance on 2016-09-16, under 510(k) number K153654.
Who is the listed applicant for Sentry WEB SmartInterp?
The FDA 510(k) record lists Carefusion Germany 234 GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sentry WEB SmartInterp?
The FDA product code for Sentry WEB SmartInterp is DQK.
相關臨床試驗
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相關器械（代碼：DQK）
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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