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FDA 510(k)

Kuschall Advance Manual Wheelchair

K-Number: K162696 · 2016-12-28

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

Device Summary

Kuschall Advance Manual Wheelchair is a medical device manufactured by Invacare Corporation. It received FDA 510(k) clearance on 2016-12-28 under approval number K162696. 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 Advance Manual Wheelchair?

Kuschall Advance 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 K162696.

When was Kuschall Advance Manual Wheelchair approved by the FDA?

Kuschall Advance Manual Wheelchair received FDA 510(k) clearance on 2016-12-28, under approval number K162696.

What company makes Kuschall Advance Manual Wheelchair?

Kuschall Advance Manual Wheelchair is manufactured by Invacare Corporation.

What is the FDA product code for Kuschall Advance Manual Wheelchair?

The FDA product code for Kuschall Advance Manual Wheelchair is IOR.

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Other Devices by Invacare Corporation

K162686Kuschall Champion Manual Wheelchair K162692Kuschall K-Series Attract Manual Wheelchair K160630Invacare Platinum Mobile Oxygen Concentrator K152536MyOn HC Manual Wheelchair K170507Invacare® TDX® SP2 Power Wheelchair; TDXSP2 TDX SP2 with LiNX Electronics, TDXSP2-CG TDX SP2 Base for Single Act. System w/ Ultra Low Maxx, TDXSP2-MCG TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx K162621Invacare Tracer SX5 Manual Wheelchair, Invacare Tracer IV Heavy Duty/Extra Wide Manual Wheelchair

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Related Devices (Code: IOR)

K162686Kuschall Champion Manual WheelchairInvacare Corporation K162692Kuschall K-Series Attract Manual WheelchairInvacare Corporation K161425APEX Manual WheelchairMotion Composites K153328SUNCO Mechanical Wheelchair, model SKW-9003Danyang Sunco Machinery Co., Ltd. K151492KuduR82 A/S K152021Pure TiltProactive Comfort, LLC

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.

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