Electric wheelchair (S7018)

FDA 510(k) K240270 · Guangdong Prestige Technology Company Limited

Substantially Equivalent

510(k) numberK240270

Submission

Device name
Electric wheelchair (S7018)
Applicant
Guangdong Prestige Technology Company Limited
Dongguan, CN
Received
January 31, 2024
Decision date
August 27, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
ITI – Wheelchair, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.3860
Specialty
Physical Medicine

A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA interprets “mobility to persons restricted to a sitting position” to mean the device type is intended to provide mobility to individuals who have mobility impairments and require an assistive device for mobility. NOTE: This type…

Other 510(k)s with product code ITI

510(k)DeviceApplicantDecision
K260229Electric wheelchair (HC819N, HC830N, HC831N)ITI · Traditional Yongkang Hengyi Vehicle Co., Ltd.09/08/2026SE
K260053Power Wheelchair (OS-R-M01I)ITI · Traditional Beijing OrionStar Technology Co., Ltd.09/08/2026SE
K261354Electric wheelchair (D03)ITI · Traditional Foshan Sowell Medical Technology Co., Ltd.08/21/2026SE
K261149Electric Wheelchair (DY611A-2, DY612A-1)ITI · Traditional Zhejiang Lumbre Electric Appliance Co., Ltd.07/10/2026SE
K261396Electric WheelchairITI · Traditional Ningbo Resshidi Medical Devices Co., Ltd.07/08/2026SE
K261164Electric wheelchair (XW-LY007 )ITI · Traditional Yongkang Ruihe Metal Product Co., Ltd.07/07/2026SE
K260937Smart Electric Wheelchair (R1-Std-BK, R1-Pro-BK, R1-Ultra-GK, R1-Ultra-WK)ITI · Traditional Shanghai Waylong Intelligent Technology Co.,Ltd06/24/2026SE
K253812Power Wheelchair (W5915B, W5915C, W5915D)ITI · Traditional Zhejiang Innuovo Rehabilitation Devices Co.,Ltd06/18/2026SE
K260335Electric Wheelchair (S500-6)ITI · Traditional Zhongshan Sulenz Intelligent Technology Co., Ltd.06/15/2026SE
K261175WHILL (WHILL Model C2)ITI · Traditional Whill, Inc.06/12/2026SE

More from Whill, Inc.

510(k)DeviceDecision
K252835Electric Scooter (S202572J, S2060, M2089, S2050)INI · Traditional 12/23/2025SE
K240272Electric Scooter (M2085, S2091)INI · Traditional 07/16/2024SE
K230001Electric Scooter (Model: M2020)INI · Traditional 07/05/2023SE
K230615Electric Scooter (Model: S3312)INI · Traditional 05/05/2023SE

Questions and answers

When was Electric wheelchair (S7018) cleared by the FDA?

Electric wheelchair (S7018) (K240270) received a 510(k) decision of Substantially Equivalent on August 27, 2024, 209 days after the submission was received.

What is the product code of K240270?

The FDA product code is ITI – Wheelchair, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.3860.