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FDA 510(k)

非侵入式血壓測量系統

K 號:K190886 · 2019-07-29

決定日期2019-07-29
產品代碼DXN
諮詢委員會履歷
決定相當於

器材摘要

Non-invasive blood pressure measurement systems is the device name listed in this FDA 510(k) record. The listed applicant is Joytech Healthcare Co. , Ltd.. It received FDA 510(k) clearance on 2019-07-29 under 510(k) number K190886. 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 Non-invasive blood pressure measurement systems?

Non-invasive blood pressure measurement systems is a medical device that received FDA 510(k) clearance on 2019-07-29. The listed applicant is Joytech Healthcare Co. , Ltd.. The 510(k) number is K190886.

When did Non-invasive blood pressure measurement systems receive FDA 510(k) clearance?

Non-invasive blood pressure measurement systems received FDA 510(k) clearance on 2019-07-29, under 510(k) number K190886.

Who is the listed applicant for Non-invasive blood pressure measurement systems?

FDA 510(k) 記錄將 Joytech Healthcare Co., Ltd. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Non-invasive blood pressure measurement systems?

The FDA product code for Non-invasive blood pressure measurement systems is DXN.

相關臨床試驗

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其他以 Joytech Healthcare Co. , Ltd. 為申請人之記錄

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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。

官方來源

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