Cleared Traditional

Electric wheelchair

K253789 · Zhejiang Yikang Medical Technology Co., Ltd. · Physical Medicine

Feb 2026

Decision

89d

Days

Class 2

Risk

About This 510(k) Submission

K253789 is an FDA 510(k) clearance for the Electric wheelchair, a Wheelchair, Powered (Class II — Special Controls, product code ITI), submitted by Zhejiang Yikang Medical Technology Co., Ltd. (Lishui, CN). The FDA issued a Cleared decision on February 25, 2026, 89 days after receiving the submission on November 28, 2025. This device falls under the Physical Medicine review panel. Regulated under 21 CFR 890.3860.

Submission Details

510(k) Number	K253789 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 28, 2025
Decision Date	February 25, 2026
Days to Decision	89 days
Submission Type	Traditional
Review Panel	Physical Medicine (PM)
Summary	Statement

Device Classification

Product Code	ITI — Wheelchair, Powered
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 890.3860
Definition	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 Of Device Is Not Intended To Climb Stairs (see Product Code: Imk).