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FDA 510(k)

Electrical Scooter, WT-T4SU

K-Number: K240590 · 2025-01-08

ApplicantW'U'S Tech Co., Ltd.
Decision Date2025-01-08
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electrical Scooter, WT-T4SU is the device name listed in this FDA 510(k) record. The listed applicant is W'U'S Tech Co., Ltd.. It received FDA 510(k) clearance on 2025-01-08 under 510(k) number K240590. 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 Electrical Scooter, WT-T4SU?

Electrical Scooter, WT-T4SU is a medical device that received FDA 510(k) clearance on 2025-01-08. The listed applicant is W'U'S Tech Co., Ltd.. The 510(k) number is K240590.

When did Electrical Scooter, WT-T4SU receive FDA 510(k) clearance?

Electrical Scooter, WT-T4SU received FDA 510(k) clearance on 2025-01-08, under 510(k) number K240590.

Who is the listed applicant for Electrical Scooter, WT-T4SU?

The FDA 510(k) record lists W'U'S Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrical Scooter, WT-T4SU?

The FDA product code for Electrical Scooter, WT-T4SU is INI.

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.

K260176Mobility Scooter (W3483, W3483A)Zhejiang Innuovo Rehabilitation Devices Co.,LtdK260094Mobility Scooter (W3465, W3902 (S50 Carbon))Zhejiang Innuovo Rehabilitation Devices Co.,LtdK261232IERO Mobility Scooter (IERO-01)Jochu Technology Co., Ltd.K261163Mobility Scooter (R200)Yongkang Ruihe Metal Product Co., Ltd.K253257Virgo Mobility Scooter (Virgo-D,Virgo-F)Jiangsu Intco Medical Products Co., Ltd.K253600Scooter (YD-03)Yurob Rehabilitation Medical Co., Ltd.

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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