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FDA 510(k)

Kuschall K-Series Attract Manual Wheelchair

K-Number: K162692 · 2016-12-28

Decision Date2016-12-28
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Kuschall K-Series Attract Manual Wheelchair is a medical device manufactured by Invacare Corporation. It received FDA 510(k) clearance on 2016-12-28 under approval number K162692. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.