數位血壓監測器
K 號：K153033 · 2016-06-24
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器材摘要
Digital Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Sunspiri Co., Ltd.. It received FDA 510(k) clearance on 2016-06-24 under 510(k) number K153033. 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 Digital Blood Pressure Monitor?
Digital Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2016-06-24. The listed applicant is Suzhou Sunspiri Co., Ltd.. The 510(k) number is K153033.
When did Digital Blood Pressure Monitor receive FDA 510(k) clearance?
Digital Blood Pressure Monitor received FDA 510(k) clearance on 2016-06-24, under 510(k) number K153033.
Who is the listed applicant for Digital Blood Pressure Monitor?
The FDA 510(k) record lists Suzhou Sunspiri Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Digital Blood Pressure Monitor?
The FDA product code for Digital Blood Pressure Monitor is DXN.
相關臨床試驗
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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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