UF(II) 寬範圍設備
K 號：K173975 · 2018-06-01
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器材摘要
UF(II) Wide Fixture is the device name listed in this FDA 510(k) record. The listed applicant is Dio Corporation. It received FDA 510(k) clearance on 2018-06-01 under 510(k) number K173975. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the UF(II) Wide Fixture?
UF(II) Wide Fixture is a medical device that received FDA 510(k) clearance on 2018-06-01. The listed applicant is Dio Corporation. The 510(k) number is K173975.
When did UF(II) Wide Fixture receive FDA 510(k) clearance?
UF(II) Wide Fixture received FDA 510(k) clearance on 2018-06-01, under 510(k) number K173975.
Who is the listed applicant for UF(II) Wide Fixture?
The FDA 510(k) record lists Dio Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UF(II) Wide Fixture?
The FDA product code for UF(II) Wide Fixture is DZE.
相關臨床試驗
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其他以 Dio Corporation 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：DZE）
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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