自動手腕藍牙血壓監測器
K 號：K170545 · 2017-11-21
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器材摘要
Automatic Wrist Bluetooth Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Truly Instrument , Ltd.. It received FDA 510(k) clearance on 2017-11-21 under 510(k) number K170545. 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 Automatic Wrist Bluetooth Blood Pressure Monitor?
Automatic Wrist Bluetooth Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2017-11-21. The listed applicant is Truly Instrument , Ltd.. The 510(k) number is K170545.
When did Automatic Wrist Bluetooth Blood Pressure Monitor receive FDA 510(k) clearance?
Automatic Wrist Bluetooth Blood Pressure Monitor received FDA 510(k) clearance on 2017-11-21, under 510(k) number K170545.
Who is the listed applicant for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA 510(k) record lists Truly Instrument , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA product code for Automatic Wrist Bluetooth 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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