FDA 510(k)

宇威®電子血壓計（YE630CR）

K 號：K252779 · 2026-03-05

申請人Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

決定日期2026-03-05

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

YUWELL® Electronic Blood Pressure Monitor (YE630CR) is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K252779. 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 YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

YUWELL® Electronic Blood Pressure Monitor (YE630CR) is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. The 510(k) number is K252779.

When did YUWELL® Electronic Blood Pressure Monitor (YE630CR) receive FDA 510(k) clearance?

YUWELL® Electronic Blood Pressure Monitor (YE630CR) received FDA 510(k) clearance on 2026-03-05, under 510(k) number K252779.

Who is the listed applicant for YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

FDA 510(k) 記錄將江蘇玉宇醫療設備與供應有限公司列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for YUWELL® Electronic Blood Pressure Monitor (YE630CR)?

The FDA product code for YUWELL® Electronic Blood Pressure Monitor (YE630CR) is DXN.

其他以 Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. 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。

K261571手動輪椅（H008，PCK7）K253228YUWELL® 電子血壓計 (YE650AR)K252805YUWELL®手指血氧計（YX105、YX106、YX110、YX310）K242736攜帶式氧氣濃縮器（Spirit-3）K250878YUWELL® 紅外線耳溫計（YHT100）；YUWELL® 紅外線耳溫計（YHT107）K213825氧濃度濃縮機型號 8F-3A，氧濃度濃縮機型號 8F-5A

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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

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