Zero Gravity Wheelchair

FDA 510(k) K931751 · General Components Intl., Inc.

Substantially Equivalent

510(k) numberK931751

Submission

Device name
Zero Gravity Wheelchair
Applicant
General Components Intl., Inc.
Salt Lake City, UT, US
Received
April 8, 1993
Decision date
July 22, 1993
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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More from Zhenjiang Assure Medical Equipment Co., Ltd.

510(k)DeviceDecision
K933051Zero Gravity Wheelchair Components, ModificationKNN · Traditional 10/12/1993SE

Questions and answers

When was Zero Gravity Wheelchair cleared by the FDA?

Zero Gravity Wheelchair (K931751) received a 510(k) decision of Substantially Equivalent on July 22, 1993, 105 days after the submission was received.

What is the product code of K931751?

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