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FDA 510(k)

Manual Wheelchair (LW01108)

K-Number: K260642 · 2026-06-02

Decision Date2026-06-02
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Manual Wheelchair (LW01108) is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Longway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K260642. 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 (LW01108)?

Manual Wheelchair (LW01108) is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is Anhui Longway Medical Technology Co., Ltd.. The 510(k) number is K260642.

When did Manual Wheelchair (LW01108) receive FDA 510(k) clearance?

Manual Wheelchair (LW01108) received FDA 510(k) clearance on 2026-06-02, under 510(k) number K260642.

Who is the listed applicant for Manual Wheelchair (LW01108)?

The FDA 510(k) record lists Anhui Longway Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Manual Wheelchair (LW01108)?

The FDA product code for Manual Wheelchair (LW01108) is IOR.

Other records listing Anhui Longway Medical 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.