電動輪椅（JLE-W01A-2023）
K 號：K240255 · 2024-08-07
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器材摘要
Electric Wheelchair (JLE-W01A-2023) is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Jianrui Technology Company Limited. It received FDA 510(k) clearance on 2024-08-07 under 510(k) number K240255. 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 Electric Wheelchair (JLE-W01A-2023)?
Electric Wheelchair (JLE-W01A-2023) is a medical device that received FDA 510(k) clearance on 2024-08-07. The listed applicant is Zhejiang Jianrui Technology Company Limited. The 510(k) number is K240255.
When did Electric Wheelchair (JLE-W01A-2023) receive FDA 510(k) clearance?
Electric Wheelchair (JLE-W01A-2023) received FDA 510(k) clearance on 2024-08-07, under 510(k) number K240255.
Who is the listed applicant for Electric Wheelchair (JLE-W01A-2023)?
The FDA 510(k) record lists Zhejiang Jianrui Technology Company Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric Wheelchair (JLE-W01A-2023)?
The FDA product code for Electric Wheelchair (JLE-W01A-2023) is 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。
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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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