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FDA 510(k)

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)

N.º K: K242789 · 2025-01-02

SolicitanteDongguan Laiguang Electronic Technology Co., Ltd.
Fecha de decisión2025-01-02
Código de productoOHS
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is the device name listed in this FDA 510(k) record. The listed applicant is Dongguan Laiguang Electronic Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-01-02 under 510(k) number K242789. 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 Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is a medical device that received FDA 510(k) clearance on 2025-01-02. The listed applicant is Dongguan Laiguang Electronic Technology Co., Ltd.. The 510(k) number is K242789.

When did Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) receive FDA 510(k) clearance?

Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) received FDA 510(k) clearance on 2025-01-02, under 510(k) number K242789.

Who is the listed applicant for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

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

What is the FDA product code for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)?

The FDA product code for Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) is OHS.

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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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