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FDA 510(k)

Light Therapy System (M500, L6)

N.º K: K251042 · 2025-06-06

SolicitanteGuangzhou Ahead Intelligent Technology Co., Ltd.
Fecha de decisión2025-06-06
Código de productoOHS
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del 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.

Preguntas frecuentes

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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Dispositivos relacionados (Código: OHS)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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