Power wheelchair (N6101)

FDA 510(k) K241686 · Zhejiang Zhonglei Medical Technology Co. , Ltd.

Substantially Equivalent

510(k) numberK241686

Submission

Device name
Power wheelchair (N6101)
Applicant
Zhejiang Zhonglei Medical Technology Co. , Ltd.
Lishui, CN
Received
June 12, 2024
Decision date
August 13, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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…

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Questions and answers

When was Power wheelchair (N6101) cleared by the FDA?

Power wheelchair (N6101) (K241686) received a 510(k) decision of Substantially Equivalent on August 13, 2024, 62 days after the submission was received.

What is the product code of K241686?

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