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FDA 510(k)

數位自動手腕式血壓監測器 MD4300

K 號:K171379 · 2018-04-10

決定日期2018-04-10
產品代碼DXN
諮詢委員會履歷
決定相當於

器材摘要

Digital Automatic Wrist Blood Pressure Monitor MD4300 is the device name listed in this FDA 510(k) record. The listed applicant is Grandway Technology (Shenzhen) Limited. It received FDA 510(k) clearance on 2018-04-10 under 510(k) number K171379. 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 Automatic Wrist Blood Pressure Monitor MD4300?

Digital Automatic Wrist Blood Pressure Monitor MD4300 is a medical device that received FDA 510(k) clearance on 2018-04-10. The listed applicant is Grandway Technology (Shenzhen) Limited. The 510(k) number is K171379.

When did Digital Automatic Wrist Blood Pressure Monitor MD4300 receive FDA 510(k) clearance?

Digital Automatic Wrist Blood Pressure Monitor MD4300 received FDA 510(k) clearance on 2018-04-10, under 510(k) number K171379.

Who is the listed applicant for Digital Automatic Wrist Blood Pressure Monitor MD4300?

The FDA 510(k) record lists Grandway Technology (Shenzhen) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Automatic Wrist Blood Pressure Monitor MD4300?

The FDA product code for Digital Automatic Wrist Blood Pressure Monitor MD4300 is DXN.

相關臨床試驗

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其他以 Grandway Technology (Shenzhen) Limited 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。

官方來源

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