eFOLDi 电动滑板车，轻便版
K号: K223492 · 2023-02-22
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决定日期2023-02-22
产品代码INI
咨询委员会PM
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决定实质等同
器械摘要
eFOLDi Scooter, Lite is the device name listed in this FDA 510(k) record. The listed applicant is Suntech UK , Ltd.. It received FDA 510(k) clearance on 2023-02-22 under 510(k) number K223492. 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 eFOLDi Scooter, Lite?
eFOLDi Scooter, Lite is a medical device that received FDA 510(k) clearance on 2023-02-22. The listed applicant is Suntech UK , Ltd.. The 510(k) number is K223492.
When did eFOLDi Scooter, Lite receive FDA 510(k) clearance?
eFOLDi Scooter, Lite received FDA 510(k) clearance on 2023-02-22, under 510(k) number K223492.
Who is the listed applicant for eFOLDi Scooter, Lite?
The FDA 510(k) record lists Suntech UK , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for eFOLDi Scooter, Lite?
The FDA product code for eFOLDi Scooter, Lite is INI.
相关临床试验
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。
列明Suntech UK , 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。
相关器械（代码：INI）
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。
K261078电动滑板车（FNS01，FNS03）Anhui Jbh Medical Apparatus Co., Ltd.K261859电动滑板车（FDB08，FDB08A，FDB12）Anhui JBH Medical Apparatus Co., Ltd.K260176移动轮椅（W3483，W3483A）Zhejiang Innuovo Rehabilitation Devices Co.,LtdK260094电动轮椅（W3465，W3902（S50碳纤维））Zhejiang Innuovo Rehabilitation Devices Co.,LtdK261232IERO 移动代步车（IERO-01）Jochu Technology Co., Ltd.K261163Mobility Scooter (R200)Yongkang Ruihe Metal Product Co., Ltd.
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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