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FDA 510(k)

Light Therapy System (M500, L6)

Número K: K251042 · 2025-06-06

RequerenteGuangzhou Ahead Intelligent Technology Co., Ltd.
Data da decisão2025-06-06
Código do produtoOHS
Comité consultivoSU
DecisãoSubstantially Equivalent

Resumo do dispositivo

Light Therapy System (M500, L6) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Ahead Intelligent Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-06-06 under 510(k) number K251042. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Light Therapy System (M500, L6)?

Light Therapy System (M500, L6) is a medical device that received FDA 510(k) clearance on 2025-06-06. The listed applicant is Guangzhou Ahead Intelligent Technology Co., Ltd.. The 510(k) number is K251042.

When did Light Therapy System (M500, L6) receive FDA 510(k) clearance?

Light Therapy System (M500, L6) received FDA 510(k) clearance on 2025-06-06, under 510(k) number K251042.

Who is the listed applicant for Light Therapy System (M500, L6)?

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

What is the FDA product code for Light Therapy System (M500, L6)?

The FDA product code for Light Therapy System (M500, L6) is OHS.

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