ENDOSEAL MTA
K 號：K170175 · 2018-02-26
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器材摘要
ENDOSEAL MTA is the device name listed in this FDA 510(k) record. The listed applicant is Maruchi. It received FDA 510(k) clearance on 2018-02-26 under 510(k) number K170175. 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 ENDOSEAL MTA?
ENDOSEAL MTA is a medical device that received FDA 510(k) clearance on 2018-02-26. The listed applicant is Maruchi. The 510(k) number is K170175.
When did ENDOSEAL MTA receive FDA 510(k) clearance?
ENDOSEAL MTA received FDA 510(k) clearance on 2018-02-26, under 510(k) number K170175.
Who is the listed applicant for ENDOSEAL MTA?
The FDA 510(k) record lists Maruchi as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSEAL MTA?
The FDA product code for ENDOSEAL MTA is KIF.
相關臨床試驗
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其他以 Maruchi 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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