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FDA 510(k)

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151

Número K: K172440 · 2018-07-13

RequerenteDongguan Prestige Sporting Goods., Ltd.
Data da decisão2018-07-13
Código do produtoINI
Comité consultivoPM
DecisãoSubstantially Equivalent

Resumo do dispositivo

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Prestige Sporting Goods., Ltd.. It received FDA 510(k) clearance on 2018-07-13 under 510(k) number K172440. 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 Solax Electric Scooter, Models: S302121, S302131, S302141, S302151?

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 is a medical device that received FDA 510(k) clearance on 2018-07-13. The listed applicant is Dongguan Prestige Sporting Goods., Ltd.. The 510(k) number is K172440.

When did Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 receive FDA 510(k) clearance?

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 received FDA 510(k) clearance on 2018-07-13, under 510(k) number K172440.

Who is the listed applicant for Solax Electric Scooter, Models: S302121, S302131, S302141, S302151?

The FDA 510(k) record lists Dongguan Prestige Sporting Goods., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Solax Electric Scooter, Models: S302121, S302131, S302141, S302151?

The FDA product code for Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 is INI.

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