Wheelchair, Mechanical Series Model 3100

FDA 510(k) K002943 · Mada Medical Products, Inc.

Substantially Equivalent

510(k) numberK002943

Submission

Device name
Wheelchair, Mechanical Series Model 3100
Applicant
Mada Medical Products, Inc.
Carlstadt, NJ, US
Received
September 21, 2000
Decision date
October 23, 2000
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 Wheelchair, Mechanical Series Model 3100 cleared by the FDA?

Wheelchair, Mechanical Series Model 3100 (K002943) received a 510(k) decision of Substantially Equivalent on October 23, 2000, 32 days after the submission was received.

What is the product code of K002943?

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