Electrically Power Wheelchairs (Models:YLB-W-0812-A01, YLB-W-0812-A02, YLB-W-0812-A03)
K-Number: K232193 · 2023-09-22
Device Summary
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.
Related Devices (Code: ITI)
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.