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FDA 510(k)

自動數位血壓監測儀 (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 及 LD-569)

K 號:K260260 · 2026-04-28

決定日期2026-04-28
產品代碼DXN
諮詢委員會履歷
決定相當於

器材摘要

Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) 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 2026-04-28 under 510(k) number K260260. 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 Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569)?

Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) is a medical device that received FDA 510(k) clearance on 2026-04-28. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K260260.

When did Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) receive FDA 510(k) clearance?

Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) received FDA 510(k) clearance on 2026-04-28, under 510(k) number K260260.

Who is the listed applicant for Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569)?

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 Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569)?

The FDA product code for Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569) 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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