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FDA 510(k)

手環自動血壓監測器(LD-735、LD-752、LD-753)

K 號:K251795 · 2025-10-09

決定日期2025-10-09
產品代碼DXN
諮詢委員會履歷
決定相當於

器材摘要

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is the device name listed in this FDA 510(k) record. The listed applicant is Honsun (Nantong) Co., Ltd.. It received FDA 510(k) clearance on 2025-10-09 under 510(k) number K251795. 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 Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is a medical device that received FDA 510(k) clearance on 2025-10-09. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K251795.

When did Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) receive FDA 510(k) clearance?

Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) received FDA 510(k) clearance on 2025-10-09, under 510(k) number K251795.

Who is the listed applicant for Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

FDA 510(k) 記錄將宏遠(南通)有限公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)?

The FDA product code for Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753) is DXN.

相關臨床試驗

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其他以 Honsun (Nantong) 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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