CP緩解棒Rx - TENS/NMES
K 號：K252236 · 2025-08-15
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器材摘要
CP Relief Wand Rx - TENS/NMES is the device name listed in this FDA 510(k) record. The listed applicant is N & C Holdings, LLC. It received FDA 510(k) clearance on 2025-08-15 under 510(k) number K252236. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CP Relief Wand Rx - TENS/NMES?
CP Relief Wand Rx - TENS/NMES is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is N & C Holdings, LLC. The 510(k) number is K252236.
When did CP Relief Wand Rx - TENS/NMES receive FDA 510(k) clearance?
CP Relief Wand Rx - TENS/NMES received FDA 510(k) clearance on 2025-08-15, under 510(k) number K252236.
Who is the listed applicant for CP Relief Wand Rx - TENS/NMES?
The FDA 510(k) record lists N & C Holdings, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CP Relief Wand Rx - TENS/NMES?
The FDA product code for CP Relief Wand Rx - TENS/NMES is GZJ.
相關臨床試驗
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相關器械（代碼：GZJ）
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
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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