Solax Electric Scooter, Models: S302121, S302131, S302141, S302151
K-Number: K172440 · 2018-07-13
Device Summary
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. 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.
Other records listing Dongguan Prestige Sporting Goods., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: INI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.