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. The listed applicant is Invacare Corporation. The 510(k) number is K162692.
When did Kuschall K-Series Attract Manual Wheelchair receive FDA 510(k) clearance?
Kuschall K-Series Attract Manual Wheelchair received FDA 510(k) clearance on 2016-12-28, under 510(k) number K162692.
Who is the listed applicant for Kuschall K-Series Attract Manual Wheelchair?
The FDA 510(k) record lists Invacare Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Invacare Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: IOR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.