電動輪椅，W5907（Q50 R碳纖維）
K 號：K220740 · 2022-05-12
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器材摘要
Power Wheelchair, W5907 (Q50 R Carbon) is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. It received FDA 510(k) clearance on 2022-05-12 under 510(k) number K220740. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Power Wheelchair, W5907 (Q50 R Carbon)?
Power Wheelchair, W5907 (Q50 R Carbon) is a medical device that received FDA 510(k) clearance on 2022-05-12. The listed applicant is Zhejiang Innuovo Rehabilitation Devices Co.,Ltd. The 510(k) number is K220740.
When did Power Wheelchair, W5907 (Q50 R Carbon) receive FDA 510(k) clearance?
Power Wheelchair, W5907 (Q50 R Carbon) received FDA 510(k) clearance on 2022-05-12, under 510(k) number K220740.
Who is the listed applicant for Power Wheelchair, W5907 (Q50 R Carbon)?
FDA 510(k) 記錄將浙江英努歐康復設備有限公司列為申請人。這並不單獨確立設備製造商的身份。
What is the FDA product code for Power Wheelchair, W5907 (Q50 R Carbon)?
The FDA product code for Power Wheelchair, W5907 (Q50 R Carbon) is ITI.
相關臨床試驗
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其他以 Zhejiang Innuovo Rehabilitation Devices Co.,Ltd 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：ITI）
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。
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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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