Nuvola
K 號：K222418 · 2022-10-07
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器材摘要
Nuvola is the device name listed in this FDA 510(k) record. The listed applicant is Gruppo Europeo Ortodonzia Srl. It received FDA 510(k) clearance on 2022-10-07 under 510(k) number K222418. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nuvola?
Nuvola is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Gruppo Europeo Ortodonzia Srl. The 510(k) number is K222418.
When did Nuvola receive FDA 510(k) clearance?
Nuvola received FDA 510(k) clearance on 2022-10-07, under 510(k) number K222418.
Who is the listed applicant for Nuvola?
The FDA 510(k) record lists Gruppo Europeo Ortodonzia Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nuvola?
The FDA product code for Nuvola is NXC.
相關臨床試驗
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相關器械（代碼：NXC）
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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