ViMove2
K 號：K163150 · 2017-07-14
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器材摘要
ViMove2 is the device name listed in this FDA 510(k) record. The listed applicant is Dorsavi, Ltd.. It received FDA 510(k) clearance on 2017-07-14 under 510(k) number K163150. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ViMove2?
ViMove2 is a medical device that received FDA 510(k) clearance on 2017-07-14. The listed applicant is Dorsavi, Ltd.. The 510(k) number is K163150.
When did ViMove2 receive FDA 510(k) clearance?
ViMove2 received FDA 510(k) clearance on 2017-07-14, under 510(k) number K163150.
Who is the listed applicant for ViMove2?
The FDA 510(k) record lists Dorsavi, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ViMove2?
The FDA product code for ViMove2 is IKN.
相關臨床試驗
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相關器械（代碼：IKN）
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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