Solax Electric Scooter (Model: S202261B)
K-Number: K202549 · 2021-02-26
Decision Date2021-02-26
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Solax Electric Scooter (Model: S202261B) is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-02-26 under approval number K202549. 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 (Model: S202261B)?
Solax Electric Scooter (Model: S202261B) is a medical device that received FDA 510(k) clearance on 2021-02-26. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K202549.
When was Solax Electric Scooter (Model: S202261B) approved by the FDA?
Solax Electric Scooter (Model: S202261B) received FDA 510(k) clearance on 2021-02-26, under approval number K202549.
What company makes Solax Electric Scooter (Model: S202261B)?
Solax Electric Scooter (Model: S202261B) is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..
What is the FDA product code for Solax Electric Scooter (Model: S202261B)?
The FDA product code for Solax Electric Scooter (Model: S202261B) is INI.
Related Clinical Trials
Other Devices by Dongguan Prestige Sporting Goods Co., Ltd.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.