FDA 510(k)

Electric Scooter (Mojo-T580)

Número K: K252347 · 2026-01-29

RequerenteDongguan Smarfody Mobility Technology Co., Ltd.

Data da decisão2026-01-29

Código do produtoINI

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do dispositivo

Electric Scooter (Mojo-T580) is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Smarfody Mobility Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-01-29 under 510(k) number K252347. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Electric Scooter (Mojo-T580)?

Electric Scooter (Mojo-T580) is a medical device that received FDA 510(k) clearance on 2026-01-29. The listed applicant is Dongguan Smarfody Mobility Technology Co., Ltd.. The 510(k) number is K252347.

When did Electric Scooter (Mojo-T580) receive FDA 510(k) clearance?

Electric Scooter (Mojo-T580) received FDA 510(k) clearance on 2026-01-29, under 510(k) number K252347.

Who is the listed applicant for Electric Scooter (Mojo-T580)?

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

What is the FDA product code for Electric Scooter (Mojo-T580)?

The FDA product code for Electric Scooter (Mojo-T580) is INI.

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Outros registros que listam Dongguan Smarfody Mobility Technology Co., Ltd. como candidato(a)

K252349Electric Scooter (Mojo-T330)

Dispositivos Relacionados (Código: INI)

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