FDA 510(k)

Dispositivo de Belleza LED Aglaia (BP-D2309)

N.º K: K250413 · 2025-03-18

SolicitanteShenzhen Perfect Idea Technology Limited

Fecha de decisión2025-03-18

Código de productoOHS

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Aglaia LED Beauty Device (BP-D2309) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Perfect Idea Technology Limited. It received FDA 510(k) clearance on 2025-03-18 under 510(k) number K250413. 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 Aglaia LED Beauty Device (BP-D2309)?

Aglaia LED Beauty Device (BP-D2309) is a medical device that received FDA 510(k) clearance on 2025-03-18. The listed applicant is Shenzhen Perfect Idea Technology Limited. The 510(k) number is K250413.

When did Aglaia LED Beauty Device (BP-D2309) receive FDA 510(k) clearance?

Aglaia LED Beauty Device (BP-D2309) received FDA 510(k) clearance on 2025-03-18, under 510(k) number K250413.

Who is the listed applicant for Aglaia LED Beauty Device (BP-D2309)?

The FDA 510(k) record lists Shenzhen Perfect Idea Technology Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Aglaia LED Beauty Device (BP-D2309)?

The FDA product code for Aglaia LED Beauty Device (BP-D2309) is OHS.

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Fuente oficial

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