Neodent植牙系統 - Neodent Acqua植牙之有效期限變更
K 號:K193592 · 2020-04-28
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器材摘要
常見問題
What is the Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is a medical device that received FDA 510(k) clearance on 2020-04-28. The listed applicant is Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K193592.
When did Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants receive FDA 510(k) clearance?
Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants received FDA 510(k) clearance on 2020-04-28, under 510(k) number K193592.
Who is the listed applicant for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
The FDA 510(k) record lists Jjgc Industria E Comercio DE Materiais Dentarios S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
The FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is DZE.
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其他以 Jjgc Industria E Comercio DE Materiais Dentarios S.A. 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:DZE)
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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