杜拉塞塔爾
K 號：K172407 · 2017-11-02
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器材摘要
Duracetal is the device name listed in this FDA 510(k) record. The listed applicant is The Myerson Company Limited. It received FDA 510(k) clearance on 2017-11-02 under 510(k) number K172407. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Duracetal?
Duracetal is a medical device that received FDA 510(k) clearance on 2017-11-02. The listed applicant is The Myerson Company Limited. The 510(k) number is K172407.
When did Duracetal receive FDA 510(k) clearance?
Duracetal received FDA 510(k) clearance on 2017-11-02, under 510(k) number K172407.
Who is the listed applicant for Duracetal?
The FDA 510(k) record lists The Myerson Company Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Duracetal?
The FDA product code for Duracetal is EBI.
相關臨床試驗
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相關器械（代碼：EBI）
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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