DIA-ROOT 生物 MTA
K 號：K200174 · 2020-09-18
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器材摘要
DIA-ROOT BIO MTA is the device name listed in this FDA 510(k) record. The listed applicant is DiaDent Group International. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K200174. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the DIA-ROOT BIO MTA?
DIA-ROOT BIO MTA is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is DiaDent Group International. The 510(k) number is K200174.
When did DIA-ROOT BIO MTA receive FDA 510(k) clearance?
DIA-ROOT BIO MTA received FDA 510(k) clearance on 2020-09-18, under 510(k) number K200174.
Who is the listed applicant for DIA-ROOT BIO MTA?
FDA 510(k) 記錄將 DiaDent Group International 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for DIA-ROOT BIO MTA?
The FDA product code for DIA-ROOT BIO MTA is KIF.
其他以 DiaDent Group International 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：KIF）
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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