Dalton Folding Wheelchairs

FDA 510(k) K850178 · Dalton Instrument Corp.

Substantially Equivalent

510(k) numberK850178

Submission

Device name
Dalton Folding Wheelchairs
Applicant
Dalton Instrument Corp.
Richardson, TX, US
Received
January 17, 1985
Decision date
April 25, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IOR – Wheelchair, Mechanical
Device class
Class I (low risk)
Regulation
21 CFR 890.3850
Specialty
Physical Medicine

A mechanical wheelchair is a manually 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/or require an assistive device for mobility.

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Questions and answers

When was Dalton Folding Wheelchairs cleared by the FDA?

Dalton Folding Wheelchairs (K850178) received a 510(k) decision of Substantially Equivalent on April 25, 1985, 98 days after the submission was received.

What is the product code of K850178?

The FDA product code is IOR – Wheelchair, Mechanical, a Class I (low risk) device regulated under 21 CFR 890.3850.