肌肉刺激器設備（PZ-100）
K 號：K250038 · 2025-05-19
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器材摘要
Muscle Stimulator Device (PZ-100) is the device name listed in this FDA 510(k) record. The listed applicant is Zhengzhou PZ Laser Slim Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-05-19 under 510(k) number K250038. 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 Muscle Stimulator Device (PZ-100)?
Muscle Stimulator Device (PZ-100) is a medical device that received FDA 510(k) clearance on 2025-05-19. The listed applicant is Zhengzhou PZ Laser Slim Technology Co., Ltd.. The 510(k) number is K250038.
When did Muscle Stimulator Device (PZ-100) receive FDA 510(k) clearance?
Muscle Stimulator Device (PZ-100) received FDA 510(k) clearance on 2025-05-19, under 510(k) number K250038.
Who is the listed applicant for Muscle Stimulator Device (PZ-100)?
FDA 510(k) 記錄將鄭州PZ雷射瘦身技術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 Muscle Stimulator Device (PZ-100)?
The FDA product code for Muscle Stimulator Device (PZ-100) is NGX.
相關臨床試驗
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其他以 Zhengzhou PZ Laser Slim 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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