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FDA 510(k)

Electric Wheelchair (LW01301A07)

K-Number: K250366 · 2025-04-08

ApplicantAnhui Longway Medical Technology Co., Ltd.
Decision Date2025-04-08
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair (LW01301A07) is a medical device manufactured by Anhui Longway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-04-08 under approval number K250366. 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 Electric Wheelchair (LW01301A07)?

Electric Wheelchair (LW01301A07) is a medical device that received FDA 510(k) clearance on 2025-04-08. It is manufactured by Anhui Longway Medical Technology Co., Ltd.. The 510(k) number is K250366.

When was Electric Wheelchair (LW01301A07) approved by the FDA?

Electric Wheelchair (LW01301A07) received FDA 510(k) clearance on 2025-04-08, under approval number K250366.

What company makes Electric Wheelchair (LW01301A07)?

Electric Wheelchair (LW01301A07) is manufactured by Anhui Longway Medical Technology Co., Ltd..

What is the FDA product code for Electric Wheelchair (LW01301A07)?

The FDA product code for Electric Wheelchair (LW01301A07) is ITI.

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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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