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FDA 510(k)

Walking rehabilitation training electric wheelchair (ZW518)

K-Number: K243783 · 2025-03-12

ApplicantShenzhen Zuowei Technology Co., Ltd.
Decision Date2025-03-12
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Walking rehabilitation training electric wheelchair (ZW518) is a medical device manufactured by Shenzhen Zuowei Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-03-12 under approval number K243783. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Walking rehabilitation training electric wheelchair (ZW518)?

Walking rehabilitation training electric wheelchair (ZW518) is a medical device that received FDA 510(k) clearance on 2025-03-12. It is manufactured by Shenzhen Zuowei Technology Co., Ltd.. The 510(k) number is K243783.

When was Walking rehabilitation training electric wheelchair (ZW518) approved by the FDA?

Walking rehabilitation training electric wheelchair (ZW518) received FDA 510(k) clearance on 2025-03-12, under approval number K243783.

What company makes Walking rehabilitation training electric wheelchair (ZW518)?

Walking rehabilitation training electric wheelchair (ZW518) is manufactured by Shenzhen Zuowei Technology Co., Ltd..

What is the FDA product code for Walking rehabilitation training electric wheelchair (ZW518)?

The FDA product code for Walking rehabilitation training electric wheelchair (ZW518) is IPL.

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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.

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