Solax Electric Scooter
K-Number: K192190 · 2021-04-23
Decision Date2021-04-23
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
Solax Electric Scooter is a medical device manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. It received FDA 510(k) clearance on 2021-04-23 under approval number K192190. 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?
Solax Electric Scooter is a medical device that received FDA 510(k) clearance on 2021-04-23. It is manufactured by Dongguan Prestige Sporting Goods Co., Ltd.. The 510(k) number is K192190.
When was Solax Electric Scooter approved by the FDA?
Solax Electric Scooter received FDA 510(k) clearance on 2021-04-23, under approval number K192190.
What company makes Solax Electric Scooter?
Solax Electric Scooter is manufactured by Dongguan Prestige Sporting Goods Co., Ltd..
What is the FDA product code for Solax Electric Scooter?
The FDA product code for Solax Electric Scooter is INI.
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.