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FDA 510(k)

Weely Manual Wheelchair

K-Number: K152827 · 2016-02-19

ApplicantRupiani
Decision Date2016-02-19
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Weely Manual Wheelchair is a medical device manufactured by Rupiani. It received FDA 510(k) clearance on 2016-02-19 under approval number K152827. 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 Weely Manual Wheelchair?

Weely Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2016-02-19. It is manufactured by Rupiani. The 510(k) number is K152827.

When was Weely Manual Wheelchair approved by the FDA?

Weely Manual Wheelchair received FDA 510(k) clearance on 2016-02-19, under approval number K152827.

What company makes Weely Manual Wheelchair?

Weely Manual Wheelchair is manufactured by Rupiani.

What is the FDA product code for Weely Manual Wheelchair?

The FDA product code for Weely Manual Wheelchair is IOR.

Related Clinical Trials

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Related Devices (Code: IOR)

K162696Kuschall Advance Manual WheelchairInvacare Corporation 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

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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