priti多達斯 ZrO2 高透明度
K 號：K161025 · 2017-02-03
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器材摘要
priti multidisc ZrO2 High Translucent is the device name listed in this FDA 510(k) record. The listed applicant is Pritidenta GmbH. It received FDA 510(k) clearance on 2017-02-03 under 510(k) number K161025. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the priti multidisc ZrO2 High Translucent?
priti multidisc ZrO2 High Translucent is a medical device that received FDA 510(k) clearance on 2017-02-03. The listed applicant is Pritidenta GmbH. The 510(k) number is K161025.
When did priti multidisc ZrO2 High Translucent receive FDA 510(k) clearance?
priti multidisc ZrO2 High Translucent received FDA 510(k) clearance on 2017-02-03, under 510(k) number K161025.
Who is the listed applicant for priti multidisc ZrO2 High Translucent?
The FDA 510(k) record lists Pritidenta GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for priti multidisc ZrO2 High Translucent?
The FDA product code for priti multidisc ZrO2 High Translucent is EIH.
相關臨床試驗
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相關器械（代碼：EIH）
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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