XLT, Rea Comfort, Spirea, Zoom

FDA 510(k) K943936 · Electric Mobility Corp.

Substantially Equivalent

510(k) numberK943936

Submission

Device name
XLT, Rea Comfort, Spirea, Zoom
Applicant
Electric Mobility Corp.
Sewell, NJ, US
Received
August 12, 1994
Decision date
September 21, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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 XLT, Rea Comfort, Spirea, Zoom cleared by the FDA?

XLT, Rea Comfort, Spirea, Zoom (K943936) received a 510(k) decision of Substantially Equivalent on September 21, 1994, 40 days after the submission was received.

What is the product code of K943936?

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