Kuschall K-Series Attract Manual Wheelchair
K-Number: K162692 · 2016-12-28
Device Summary
Frequently Asked Questions
What is the Kuschall K-Series Attract Manual Wheelchair?
Kuschall K-Series Attract Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2016-12-28. It is manufactured by Invacare Corporation. The 510(k) number is K162692.
When was Kuschall K-Series Attract Manual Wheelchair approved by the FDA?
Kuschall K-Series Attract Manual Wheelchair received FDA 510(k) clearance on 2016-12-28, under approval number K162692.
What company makes Kuschall K-Series Attract Manual Wheelchair?
Kuschall K-Series Attract Manual Wheelchair is manufactured by Invacare Corporation.
What is the FDA product code for Kuschall K-Series Attract Manual Wheelchair?
The FDA product code for Kuschall K-Series Attract Manual Wheelchair is IOR.
Related Clinical Trials
Other Devices by Invacare Corporation
Related Devices (Code: IOR)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.