FDA 510(k)

Electric Wheelchair

Número K: K262054 · 2026-09-16

RequerenteYongkang Joymax Medical Technology Co., Ltd.

Data da decisão2026-09-16

Código do produtoITI

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electric Wheelchair is the device name listed in this FDA 510(k) record. The listed applicant is Yongkang Joymax Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-09-16 under 510(k) number K262054. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electric Wheelchair?

Cadeira de Rodas Elétrica é um dispositivo médico que recebeu aprovação da FDA 510(k) em 16 de setembro de 2026. O solicitante listado é Yongkang Joymax Medical Technology Co., Ltd.. O número 510(k) é K262054.

When did Electric Wheelchair receive FDA 510(k) clearance?

Electric Wheelchair received FDA 510(k) clearance on 2026-09-16, under 510(k) number K262054.

Who is the listed applicant for Electric Wheelchair?

The FDA 510(k) record lists Yongkang Joymax Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electric Wheelchair?

The FDA product code for Electric Wheelchair is ITI.

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Dispositivos Relacionados (Código: ITI)

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Fonte oficial

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