7000 Series Lightweight Wheelchair, Models 7160L, 7180L and 7200L

FDA 510(k) K061273 · Nova Ortho-Med, Inc.

Substantially Equivalent

510(k) numberK061273

Submission

Device name
7000 Series Lightweight Wheelchair, Models 7160L, 7180L and 7200L
Applicant
Nova Ortho-Med, Inc.
Gardena, CA, US
Received
May 8, 2006
Decision date
May 23, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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 7000 Series Lightweight Wheelchair, Models 7160L, 7180L and 7200L cleared by the FDA?

7000 Series Lightweight Wheelchair, Models 7160L, 7180L and 7200L (K061273) received a 510(k) decision of Substantially Equivalent on May 23, 2006, 15 days after the submission was received.

What is the product code of K061273?

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