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FDA 510(k)

Diode Laser Therapy Device (DF-DIODE LASER-S1)

N.º K: K241547 · 2024-08-13

SolicitanteWeifang Dragonfly Electronics Technology Co., Ltd.
Fecha de decisión2024-08-13
Código de productoGEX
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Diode Laser Therapy Device (DF-DIODE LASER-S1) is the device name listed in this FDA 510(k) record. The listed applicant is Weifang Dragonfly Electronics Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-08-13 under 510(k) number K241547. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Diode Laser Therapy Device (DF-DIODE LASER-S1)?

Diode Laser Therapy Device (DF-DIODE LASER-S1) is a medical device that received FDA 510(k) clearance on 2024-08-13. The listed applicant is Weifang Dragonfly Electronics Technology Co., Ltd.. The 510(k) number is K241547.

When did Diode Laser Therapy Device (DF-DIODE LASER-S1) receive FDA 510(k) clearance?

Diode Laser Therapy Device (DF-DIODE LASER-S1) received FDA 510(k) clearance on 2024-08-13, under 510(k) number K241547.

Who is the listed applicant for Diode Laser Therapy Device (DF-DIODE LASER-S1)?

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

What is the FDA product code for Diode Laser Therapy Device (DF-DIODE LASER-S1)?

The FDA product code for Diode Laser Therapy Device (DF-DIODE LASER-S1) is GEX. This falls under the Gastroenterology category.

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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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