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FDA 510(k)

Manual Wheelchair (MS01);Manual Wheelchair (MA01)

K-Number: K261075 · 2026-06-22

Decision Date2026-06-22
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Manual Wheelchair (MS01);Manual Wheelchair (MA01) is the device name listed in this FDA 510(k) record. The listed applicant is GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-06-22 under 510(k) number K261075. 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 (MS01);Manual Wheelchair (MA01)?

Manual Wheelchair (MS01);Manual Wheelchair (MA01) is a medical device that received FDA 510(k) clearance on 2026-06-22. The listed applicant is GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.. The 510(k) number is K261075.

When did Manual Wheelchair (MS01);Manual Wheelchair (MA01) receive FDA 510(k) clearance?

Manual Wheelchair (MS01);Manual Wheelchair (MA01) received FDA 510(k) clearance on 2026-06-22, under 510(k) number K261075.

Who is the listed applicant for Manual Wheelchair (MS01);Manual Wheelchair (MA01)?

The FDA 510(k) record lists GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Manual Wheelchair (MS01);Manual Wheelchair (MA01)?

The FDA product code for Manual Wheelchair (MS01);Manual Wheelchair (MA01) is IOR.

Other records listing GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: IOR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.