Invacare® Solara® 3G 及 Solara® 3G Spree 手動輪椅手冊
K 號:K181090 · 2018-11-14
廣告
器材摘要
常見問題
What is the Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?
Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is a medical device that received FDA 510(k) clearance on 2018-11-14. The listed applicant is Invacare Corporation. The 510(k) number is K181090.
When did Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs receive FDA 510(k) clearance?
Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs received FDA 510(k) clearance on 2018-11-14, under 510(k) number K181090.
Who is the listed applicant for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?
The FDA 510(k) record lists Invacare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?
The FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is IOR.
相關臨床試驗
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。
其他以 Invacare 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:IOR)
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。
廣告