電擊治療與電動肌肉刺激器
K 號：K251706 · 2025-07-30
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器材摘要
TENS and EMS Unit is the device name listed in this FDA 510(k) record. The listed applicant is Changsha Anxiang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-07-30 under 510(k) number K251706. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TENS and EMS Unit?
TENS and EMS Unit is a medical device that received FDA 510(k) clearance on 2025-07-30. The listed applicant is Changsha Anxiang Medical Technology Co., Ltd.. The 510(k) number is K251706.
When did TENS and EMS Unit receive FDA 510(k) clearance?
TENS and EMS Unit received FDA 510(k) clearance on 2025-07-30, under 510(k) number K251706.
Who is the listed applicant for TENS and EMS Unit?
The FDA 510(k) record lists Changsha Anxiang Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TENS and EMS Unit?
The FDA product code for TENS and EMS Unit is NGX.
其他以 Changsha Anxiang Medical Technology 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。
相關器械（代碼：NGX）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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