Cleared Traditional

K253307 - Electric wheelchair (FDA 510(k) Clearance)

Mar 2026
Decision
179d
Days
Class 2
Risk

K253307 is an FDA 510(k) clearance for the Electric wheelchair. This device is classified as a Wheelchair, Powered (Class II - Special Controls, product code ITI).

Submitted by Foshan Dahao Medical Technology Co., Ltd. (Foshan, CN). The FDA issued a Cleared decision on March 27, 2026, 179 days after receiving the submission on September 29, 2025.

This device falls under the Physical Medicine FDA review panel. Regulated under 21 CFR 890.3860. 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)..

Submission Details

510(k) Number K253307 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2025
Decision Date March 27, 2026
Days to Decision 179 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF

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).

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