Handi-Traction

FDA 510(k) K904862 · Handi-Trak, Inc.

Substantially Equivalent

510(k) numberK904862

Submission

Device name
Handi-Traction
Applicant
Handi-Trak, Inc.
West Allis, WI, US
Received
October 29, 1990
Decision date
November 5, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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More from Whill, Inc.

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K904913Handi-Trak Wheelchair Snow ChainsKNN · Traditional 11/07/1990SE

Questions and answers

When was Handi-Traction cleared by the FDA?

Handi-Traction (K904862) received a 510(k) decision of Substantially Equivalent on November 5, 1990, 7 days after the submission was received.

What is the product code of K904862?

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