FDA 510(k)Electric Scooter (FNS01,FNS03)
K 號：K261078 · 2026-09-24
決定日期2026-09-24
產品代碼INI
諮詢委員會PM
決定Substantially Equivalent
器材摘要
Electric Scooter (FNS01,FNS03) is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Jbh Medical Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2026-09-24 under 510(k) number K261078. 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 Electric Scooter (FNS01,FNS03)?
Electric Scooter (FNS01,FNS03) is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Anhui Jbh Medical Apparatus Co., Ltd.. The 510(k) number is K261078.
電動滑板車（FNS01,FNS03）是什麼時候獲得FDA 510(k)許可的？
Electric Scooter (FNS01,FNS03) received FDA 510(k) clearance on 2026-09-24, under 510(k) number K261078.
Who is the listed applicant for Electric Scooter (FNS01,FNS03)?
The FDA 510(k) record lists Anhui Jbh Medical Apparatus Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Electric Scooter (FNS01,FNS03)?
The FDA product code for Electric Scooter (FNS01,FNS03) is INI.
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其他以 Anhui Jbh Medical Apparatus Co., Ltd. 為申請人之記錄
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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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