Martin Chair, Model C4S1

FDA 510(k) K080506 · Martin Manufacturing Co., LLC

Substantially Equivalent

510(k) numberK080506

Submission

Device name
Martin Chair, Model C4S1
Applicant
Martin Manufacturing Co., LLC
Raleigh, NC, US
Received
February 25, 2008
Decision date
June 9, 2008
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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 Martin Chair, Model C4S1 cleared by the FDA?

Martin Chair, Model C4S1 (K080506) received a 510(k) decision of Substantially Equivalent on June 9, 2008, 105 days after the submission was received.

What is the product code of K080506?

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