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FDA 510(k)

Walking rehabilitation training electric wheelchair (ZW518)

Número K: K243783 · 2025-03-12

RequerenteShenzhen Zuowei Technology Co., Ltd.
Data da decisão2025-03-12
Código do produtoIPL
Comité consultivoPM
DecisãoSubstantially Equivalent

Resumo do dispositivo

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

Perguntas frequentes

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. The listed applicant is Shenzhen Zuowei Technology Co., Ltd.. The 510(k) number is K243783.

When did Walking rehabilitation training electric wheelchair (ZW518) receive FDA 510(k) clearance?

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

Who is the listed applicant for Walking rehabilitation training electric wheelchair (ZW518)?

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

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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