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FDA 510(k)

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

K-Number: K172440 · 2018-07-13

ApplicantDongguan Prestige Sporting Goods., Ltd.
Decision Date2018-07-13
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 is a medical device manufactured by Dongguan Prestige Sporting Goods., Ltd.. It received FDA 510(k) clearance on 2018-07-13 under approval number K172440. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

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. It is manufactured by Dongguan Prestige Sporting Goods., Ltd.. The 510(k) number is K172440.

When was Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 approved by the FDA?

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

What company makes Solax Electric Scooter, Models: S302121, S302131, S302141, S302151?

Solax Electric Scooter, Models: S302121, S302131, S302141, S302151 is manufactured by Dongguan Prestige Sporting Goods., Ltd..

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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