QX鏈接
K 號：K161113 · 2016-08-05
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器材摘要
QXLink is the device name listed in this FDA 510(k) record. The listed applicant is Vieworks Co., Ltd.. It received FDA 510(k) clearance on 2016-08-05 under 510(k) number K161113. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the QXLink?
QXLink is a medical device that received FDA 510(k) clearance on 2016-08-05. The listed applicant is Vieworks Co., Ltd.. The 510(k) number is K161113.
When did QXLink receive FDA 510(k) clearance?
QXLink received FDA 510(k) clearance on 2016-08-05, under 510(k) number K161113.
Who is the listed applicant for QXLink?
The FDA 510(k) record lists Vieworks Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QXLink?
The FDA product code for QXLink is LLZ.
相關臨床試驗
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其他以 Vieworks Co., Ltd. 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：LLZ）
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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