FDA 510(k)

Solax Electric Scooter (Models: S204311M, S204161, S204143)

Número K: K190737 · 2021-05-10

RequerenteDongguan Prestige Sporting Goods Co., Ltd.

Data da decisão2021-05-10

Código do produtoINI

Comité consultivoPM

DecisãoSubstantially Equivalent

Resumo do dispositivo

Solax Electric Scooter (Models: S204311M, S204161, S204143) is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-05-10 under 510(k) number K190737. 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: S204311M, S204161, S204143)?

Solax Electric Scooter (Models: S204311M, S204161, S204143) is a medical device that received FDA 510(k) clearance on 2021-05-10. The listed applicant is Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K190737.

When did Solax Electric Scooter (Models: S204311M, S204161, S204143) receive FDA 510(k) clearance?

Solax Electric Scooter (Models: S204311M, S204161, S204143) received FDA 510(k) clearance on 2021-05-10, under 510(k) number K190737.

Who is the listed applicant for Solax Electric Scooter (Models: S204311M, S204161, S204143)?

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

What is the FDA product code for Solax Electric Scooter (Models: S204311M, S204161, S204143)?

The FDA product code for Solax Electric Scooter (Models: S204311M, S204161, S204143) is INI.

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