KDF 鑫鐙膚片
K 號：K221429 · 2022-07-14
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器材摘要
KDF Zirconia Disc is the device name listed in this FDA 510(k) record. The listed applicant is Denken-Highdental Co., Ltd.. It received FDA 510(k) clearance on 2022-07-14 under 510(k) number K221429. 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 KDF Zirconia Disc?
KDF Zirconia Disc is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Denken-Highdental Co., Ltd.. The 510(k) number is K221429.
When did KDF Zirconia Disc receive FDA 510(k) clearance?
KDF Zirconia Disc received FDA 510(k) clearance on 2022-07-14, under 510(k) number K221429.
Who is the listed applicant for KDF Zirconia Disc?
The FDA 510(k) record lists Denken-Highdental Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KDF Zirconia Disc?
The FDA product code for KDF Zirconia Disc 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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