Wheelchair BCW 6000

FDA 510(k) K883034 · O'Tec Corp.

Substantially Equivalent

510(k) numberK883034

Submission

Device name
Wheelchair BCW 6000
Applicant
O'Tec Corp.
Oberlin, KS, US
Received
July 19, 1988
Decision date
August 2, 1988
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 Wheelchair BCW 6000 cleared by the FDA?

Wheelchair BCW 6000 (K883034) received a 510(k) decision of Substantially Equivalent on August 2, 1988, 14 days after the submission was received.

What is the product code of K883034?

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