行動輪椅（CL-Q3，CL-Q4）
K 號：K253631 · 2026-02-23
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器材摘要
Mobility Scooter (CL-Q3, CL-Q4) is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Wei Ling New Energy Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-02-23 under 510(k) number K253631. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Mobility Scooter (CL-Q3, CL-Q4)?
Mobility Scooter (CL-Q3, CL-Q4) is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is Zhejiang Wei Ling New Energy Technology Co., Ltd.. The 510(k) number is K253631.
When did Mobility Scooter (CL-Q3, CL-Q4) receive FDA 510(k) clearance?
Mobility Scooter (CL-Q3, CL-Q4) received FDA 510(k) clearance on 2026-02-23, under 510(k) number K253631.
Who is the listed applicant for Mobility Scooter (CL-Q3, CL-Q4)?
The FDA 510(k) record lists Zhejiang Wei Ling New Energy Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Mobility Scooter (CL-Q3, CL-Q4)?
The FDA product code for Mobility Scooter (CL-Q3, CL-Q4) is INI.
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：INI）
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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