逐漸牙齒氧化鎂鋁陶瓷空白
K 號：K231687 · 2023-09-07
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器材摘要
Gradual Dental Zirconia Blank is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning Upcera Co., Ltd.. It received FDA 510(k) clearance on 2023-09-07 under 510(k) number K231687. 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 Gradual Dental Zirconia Blank?
Gradual Dental Zirconia Blank is a medical device that received FDA 510(k) clearance on 2023-09-07. The listed applicant is Liaoning Upcera Co., Ltd.. The 510(k) number is K231687.
When did Gradual Dental Zirconia Blank receive FDA 510(k) clearance?
Gradual Dental Zirconia Blank received FDA 510(k) clearance on 2023-09-07, under 510(k) number K231687.
Who is the listed applicant for Gradual Dental Zirconia Blank?
The FDA 510(k) record lists Liaoning Upcera Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gradual Dental Zirconia Blank?
The FDA product code for Gradual Dental Zirconia Blank is EIH.
相關臨床試驗
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其他以 Liaoning Upcera Co., 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：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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