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FDA 510(k)

RGK Daily Range Wheelchairs

N.º K: K200135 · 2020-09-10

SolicitanteRgk Wheelchairs, Ltd.
Fecha de decisión2020-09-10
Código de productoIOR
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del 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.

Preguntas frecuentes

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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Dispositivos relacionados (Código: IOR)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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