Voutia™
K 號：K173808 · 2018-07-27
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器材摘要
Voutia™ is the device name listed in this FDA 510(k) record. The listed applicant is Jeffrey Ward Cash, Dds. It received FDA 510(k) clearance on 2018-07-27 under 510(k) number K173808. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常見問題
What is the Voutia™?
Voutia™ is a medical device that received FDA 510(k) clearance on 2018-07-27. The listed applicant is Jeffrey Ward Cash, Dds. The 510(k) number is K173808.
When did Voutia™ receive FDA 510(k) clearance?
Voutia™ received FDA 510(k) clearance on 2018-07-27, under 510(k) number K173808.
Who is the listed applicant for Voutia™?
The FDA 510(k) record lists Jeffrey Ward Cash, Dds as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Voutia™?
The FDA product code for Voutia™ is LFD.
相關臨床試驗
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相關器械（代碼：LFD）
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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