RGK 每日范围轮椅
K号: K200135 · 2020-09-10
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决定日期2020-09-10
产品代码IOR
咨询委员会PM
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决定实质等同
器械摘要
RGK Daily Range Wheelchairs is the device name listed in this FDA 510(k) record. The listed applicant is Rgk Wheelchairs, Ltd.. It received FDA 510(k) clearance on 2020-09-10 under 510(k) number K200135. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RGK Daily Range Wheelchairs?
RGK Daily Range Wheelchairs is a medical device that received FDA 510(k) clearance on 2020-09-10. The listed applicant is Rgk Wheelchairs, Ltd.. The 510(k) number is K200135.
When did RGK Daily Range Wheelchairs receive FDA 510(k) clearance?
RGK Daily Range Wheelchairs received FDA 510(k) clearance on 2020-09-10, under 510(k) number K200135.
Who is the listed applicant for RGK Daily Range Wheelchairs?
The FDA 510(k) record lists Rgk Wheelchairs, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RGK Daily Range Wheelchairs?
The FDA product code for RGK Daily Range Wheelchairs is IOR.
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相关器械（代码：IOR）
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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