氧化鋁塊
K 號：K222520 · 2022-11-14
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器材摘要
Zirconia Block is the device name listed in this FDA 510(k) record. The listed applicant is Yilink (Tianjin) Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-14 under 510(k) number K222520. 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 Zirconia Block?
Zirconia Block is a medical device that received FDA 510(k) clearance on 2022-11-14. The listed applicant is Yilink (Tianjin) Biotechnology Co., Ltd.. The 510(k) number is K222520.
When did Zirconia Block receive FDA 510(k) clearance?
Zirconia Block received FDA 510(k) clearance on 2022-11-14, under 510(k) number K222520.
Who is the listed applicant for Zirconia Block?
The FDA 510(k) record lists Yilink (Tianjin) Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Zirconia Block?
The FDA product code for Zirconia Block is EIH.
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其他以 Yilink (Tianjin) Biotechnology 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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