電子血壓監測器
K 號：K200939 · 2020-08-20
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器材摘要
Electronic Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. It received FDA 510(k) clearance on 2020-08-20 under 510(k) number K200939. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Electronic Blood Pressure Monitor?
Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-08-20. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. The 510(k) number is K200939.
When did Electronic Blood Pressure Monitor receive FDA 510(k) clearance?
Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2020-08-20, under 510(k) number K200939.
Who is the listed applicant for Electronic Blood Pressure Monitor?
FDA 510(k) 記錄將江蘇玉宇醫療設備與供應有限公司列為申請人。這並不單獨確立設備製造商的身份。
What is the FDA product code for Electronic Blood Pressure Monitor?
The FDA product code for Electronic Blood Pressure Monitor is DXN.
相關臨床試驗
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其他以 Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. 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：DXN）
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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