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K 號：K161892 · 2017-03-02
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器材摘要
Slimming Treatment Device is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Honkon Technologies Co., Ltd.. It received FDA 510(k) clearance on 2017-03-02 under 510(k) number K161892. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Slimming Treatment Device?
Slimming Treatment Device is a medical device that received FDA 510(k) clearance on 2017-03-02. The listed applicant is Beijing Honkon Technologies Co., Ltd.. The 510(k) number is K161892.
When did Slimming Treatment Device receive FDA 510(k) clearance?
Slimming Treatment Device received FDA 510(k) clearance on 2017-03-02, under 510(k) number K161892.
Who is the listed applicant for Slimming Treatment Device?
The FDA 510(k) record lists Beijing Honkon Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Slimming Treatment Device?
The FDA product code for Slimming Treatment Device is NUV.
相關臨床試驗
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相關器械（代碼：NUV）
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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