RELI REDIDIOX 着色，RELI REDIDIOX，RELI REDIDIOX 未着色
K 號：K161737 · 2017-03-02
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器材摘要
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical. It received FDA 510(k) clearance on 2017-03-02 under 510(k) number K161737. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is a medical device that received FDA 510(k) clearance on 2017-03-02. The listed applicant is Myco Medical. The 510(k) number is K161737.
When did RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed receive FDA 510(k) clearance?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed received FDA 510(k) clearance on 2017-03-02, under 510(k) number K161737.
Who is the listed applicant for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
The FDA 510(k) record lists Myco Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
The FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is NEW.
相關臨床試驗
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相關器械（代碼：NEW）
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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