維爾美尼牙醫用設備（V4D）
K 號：K240003 · 2024-08-30
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器材摘要
Velmeni for Dentists (V4D) is the device name listed in this FDA 510(k) record. The listed applicant is Velmeni, Inc.. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K240003. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Velmeni for Dentists (V4D)?
Velmeni for Dentists (V4D) is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Velmeni, Inc.. The 510(k) number is K240003.
When did Velmeni for Dentists (V4D) receive FDA 510(k) clearance?
Velmeni for Dentists (V4D) received FDA 510(k) clearance on 2024-08-30, under 510(k) number K240003.
Who is the listed applicant for Velmeni for Dentists (V4D)?
FDA 510(k) 記錄將 Velmeni, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for Velmeni for Dentists (V4D)?
The FDA product code for Velmeni for Dentists (V4D) is MYN.
相關臨床試驗
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。
其他以 Velmeni, Inc. 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：MYN）
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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