維特歐防霧溶液
K 號：K163257 · 2017-05-24
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器材摘要
VitreOx Anti-fog Solution is the device name listed in this FDA 510(k) record. The listed applicant is Sio2 Nanotech, LLC. It received FDA 510(k) clearance on 2017-05-24 under 510(k) number K163257. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VitreOx Anti-fog Solution?
VitreOx Anti-fog Solution is a medical device that received FDA 510(k) clearance on 2017-05-24. The listed applicant is Sio2 Nanotech, LLC. The 510(k) number is K163257.
When did VitreOx Anti-fog Solution receive FDA 510(k) clearance?
VitreOx Anti-fog Solution received FDA 510(k) clearance on 2017-05-24, under 510(k) number K163257.
Who is the listed applicant for VitreOx Anti-fog Solution?
The FDA 510(k) record lists Sio2 Nanotech, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VitreOx Anti-fog Solution?
The FDA product code for VitreOx Anti-fog Solution is OCT.
相關臨床試驗
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相關器械（代碼：OCT）
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。
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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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