科普蘭 Zri
K 號：K232952 · 2024-06-24
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器材摘要
Copran Zri is the device name listed in this FDA 510(k) record. The listed applicant is Whitepeaks Dental Solutions GmbH. It received FDA 510(k) clearance on 2024-06-24 under 510(k) number K232952. 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 Copran Zri?
Copran Zri is a medical device that received FDA 510(k) clearance on 2024-06-24. The listed applicant is Whitepeaks Dental Solutions GmbH. The 510(k) number is K232952.
When did Copran Zri receive FDA 510(k) clearance?
Copran Zri received FDA 510(k) clearance on 2024-06-24, under 510(k) number K232952.
Who is the listed applicant for Copran Zri?
The FDA 510(k) record lists Whitepeaks Dental Solutions GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Copran Zri?
The FDA product code for Copran Zri is EIH.
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 Whitepeaks Dental Solutions GmbH 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：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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