FDA 510(k)

Electric Scooter (FNS01,FNS03)

K号: K261078 · 2026-09-24

申请人Anhui Jbh Medical Apparatus Co., Ltd.

决定日期2026-09-24

产品代码INI

咨询委员会PM

决定Substantially Equivalent

器械摘要

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.

常见问题

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.

电动滑板车（FNS01，FNS03）何时获得FDA 510(k)批准？

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.

列明Anhui Jbh Medical Apparatus Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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官方来源

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