IonoStar Plus
K 號：K160774 · 2016-08-03
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器材摘要
IonoStar Plus is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2016-08-03 under 510(k) number K160774. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the IonoStar Plus?
IonoStar Plus is a medical device that received FDA 510(k) clearance on 2016-08-03. The listed applicant is Voco GmbH. The 510(k) number is K160774.
When did IonoStar Plus receive FDA 510(k) clearance?
IonoStar Plus received FDA 510(k) clearance on 2016-08-03, under 510(k) number K160774.
Who is the listed applicant for IonoStar Plus?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IonoStar Plus?
The FDA product code for IonoStar Plus is EMA.
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其他以 Voco GmbH 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：EMA）
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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