Jewel MPS

FDA 510(k) K011374 · Vestil Manufacturing Corp.

Substantially Equivalent

510(k) numberK011374

Submission

Device name
Jewel MPS
Applicant
Vestil Manufacturing Corp.
Angola, IN, US
Received
May 4, 2001
Decision date
May 29, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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 Jewel MPS cleared by the FDA?

Jewel MPS (K011374) received a 510(k) decision of Substantially Equivalent on May 29, 2001, 25 days after the submission was received.

What is the product code of K011374?

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