電動輪椅
K 號：K261396 · 2026-07-08
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器材摘要
Electric Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Resshidi Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2026-07-08 under 510(k) number K261396. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
什麼是電動輪椅？
Electric Wheelchair is a medical device that received FDA 510(k) clearance on 2026-07-08. The listed applicant is Ningbo Resshidi Medical Devices Co., Ltd.. The 510(k) number is K261396.
電動輪椅是何時獲得FDA 510(k)許可的？
Electric Wheelchair received FDA 510(k) clearance on 2026-07-08, under 510(k) number K261396.
誰是電動輪椅的登記申請人？
The FDA 510(k) record lists Ningbo Resshidi Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
FDA電動輪椅的產品代碼是什麼？
FDA電動輪椅的產品代碼為ITI。
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。
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。
K262582電動輪椅（GP100）Suzhou Green Pine Medical Co., Ltd.K262054電動輪椅Yongkang Joymax Medical Technology Co., Ltd.K260053電動輪椅 (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229電動輪椅（HC819N、HC830N、HC831N）Yongkang Hengyi Vehicle Co., Ltd.K261354電動輪椅（D03）Foshan Sowell Medical Technology Co., Ltd.K261149電動輪椅（DY611A-2，DY612A-1）Zhejiang Lumbre Electric Appliance Co., Ltd.
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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