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FDA 510(k)

Manual Wheelchair

K-Number: K180852 · 2019-03-01

ApplicantJiangyin Newrise Medical Equipment Co., Ltd.
Decision Date2019-03-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Manual Wheelchair is a medical device manufactured by Jiangyin Newrise Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2019-03-01 under approval number K180852. 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 Manual Wheelchair?

Manual Wheelchair is a medical device that received FDA 510(k) clearance on 2019-03-01. It is manufactured by Jiangyin Newrise Medical Equipment Co., Ltd.. The 510(k) number is K180852.

When was Manual Wheelchair approved by the FDA?

Manual Wheelchair received FDA 510(k) clearance on 2019-03-01, under approval number K180852.

What company makes Manual Wheelchair?

Manual Wheelchair is manufactured by Jiangyin Newrise Medical Equipment Co., Ltd..

What is the FDA product code for Manual Wheelchair?

The FDA product code for Manual Wheelchair is IOR.

Related Clinical Trials

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Related Devices (Code: IOR)

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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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