牙醫用氧化鋁礦塊
K 號：K192262 · 2020-05-29
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器材摘要
Dental Zirconia Blocks is the device name listed in this FDA 510(k) record. The listed applicant is De Corematrix Co., Ltd.. It received FDA 510(k) clearance on 2020-05-29 under 510(k) number K192262. 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 Dental Zirconia Blocks?
Dental Zirconia Blocks is a medical device that received FDA 510(k) clearance on 2020-05-29. The listed applicant is De Corematrix Co., Ltd.. The 510(k) number is K192262.
When did Dental Zirconia Blocks receive FDA 510(k) clearance?
Dental Zirconia Blocks received FDA 510(k) clearance on 2020-05-29, under 510(k) number K192262.
Who is the listed applicant for Dental Zirconia Blocks?
The FDA 510(k) record lists De Corematrix Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental Zirconia Blocks?
The FDA product code for Dental Zirconia Blocks 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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