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FDA 510(k)

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)

K-Number: K232193 · 2023-09-22

Decision Date2023-09-22
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) is a medical device manufactured by Yurob Rehabilitation Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-09-22 under approval number K232193. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)?

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) is a medical device that received FDA 510(k) clearance on 2023-09-22. It is manufactured by Yurob Rehabilitation Medical Co., Ltd.. The 510(k) number is K232193.

When was Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) approved by the FDA?

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) received FDA 510(k) clearance on 2023-09-22, under approval number K232193.

What company makes Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)?

Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) is manufactured by Yurob Rehabilitation Medical Co., Ltd..

What is the FDA product code for Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)?

The FDA product code for Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03) is ITI.

Related Clinical Trials

Related PubMed Literature

Other Devices by Yurob Rehabilitation Medical Co., Ltd.

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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.