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FDA 510(k)

Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003)

K-Number: K250158 · 2025-04-28

ApplicantZhe Jiang Cleisman Industry and Trade Co.,Ltd
Decision Date2025-04-28
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) is a medical device manufactured by Zhe Jiang Cleisman Industry and Trade Co.,Ltd. It received FDA 510(k) clearance on 2025-04-28 under approval number K250158. 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 (ZH-W001,ZH-W002 ,ZH-W003)?

Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) is a medical device that received FDA 510(k) clearance on 2025-04-28. It is manufactured by Zhe Jiang Cleisman Industry and Trade Co.,Ltd. The 510(k) number is K250158.

When was Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) approved by the FDA?

Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) received FDA 510(k) clearance on 2025-04-28, under approval number K250158.

What company makes Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003)?

Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) is manufactured by Zhe Jiang Cleisman Industry and Trade Co.,Ltd.

What is the FDA product code for Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003)?

The FDA product code for Electric Wheelchair (ZH-W001,ZH-W002 ,ZH-W003) 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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