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FDA 510(k)

RGK Daily Range Wheelchairs

Número K: K200135 · 2020-09-10

RequerenteRgk Wheelchairs, Ltd.
Data da decisão2020-09-10
Código do produtoIOR
Comité consultivoPM
DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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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