InMode 系統搭配 vTone 濾頭
K 號：K200293 · 2020-05-05
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器材摘要
InMode System with vTone Applicator is the device name listed in this FDA 510(k) record. The listed applicant is InMode , Ltd.. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K200293. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the InMode System with vTone Applicator?
InMode System with vTone Applicator is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is InMode , Ltd.. The 510(k) number is K200293.
When did InMode System with vTone Applicator receive FDA 510(k) clearance?
InMode System with vTone Applicator received FDA 510(k) clearance on 2020-05-05, under 510(k) number K200293.
Who is the listed applicant for InMode System with vTone Applicator?
The FDA 510(k) record lists InMode , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InMode System with vTone Applicator?
The FDA product code for InMode System with vTone Applicator is KPI.
相關臨床試驗
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其他以 InMode , 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：KPI）
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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