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FDA 510(k)

Electric Scooter (S202572J, S2060, M2089, S2050)

K-Number: K252835 · 2025-12-23

ApplicantGuangdong Prestige Technology Co., Ltd.
Decision Date2025-12-23
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Scooter (S202572J, S2060, M2089, S2050) is a medical device manufactured by Guangdong Prestige Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-12-23 under approval number K252835. 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 Electric Scooter (S202572J, S2060, M2089, S2050)?

Electric Scooter (S202572J, S2060, M2089, S2050) is a medical device that received FDA 510(k) clearance on 2025-12-23. It is manufactured by Guangdong Prestige Technology Co., Ltd.. The 510(k) number is K252835.

When was Electric Scooter (S202572J, S2060, M2089, S2050) approved by the FDA?

Electric Scooter (S202572J, S2060, M2089, S2050) received FDA 510(k) clearance on 2025-12-23, under approval number K252835.

What company makes Electric Scooter (S202572J, S2060, M2089, S2050)?

Electric Scooter (S202572J, S2060, M2089, S2050) is manufactured by Guangdong Prestige Technology Co., Ltd..

What is the FDA product code for Electric Scooter (S202572J, S2060, M2089, S2050)?

The FDA product code for Electric Scooter (S202572J, S2060, M2089, S2050) is INI.

Other Devices by Guangdong Prestige Technology Co., Ltd.

K230001Electric Scooter (Model: M2020) K230615Electric Scooter (Model: S3312) K240272Electric Scooter (M2085, S2091)

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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.

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