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FDA 510(k)

Lightin System, Lightin, Lightin Generator

N.º K: K232177 · 2024-07-10

SolicitanteSolmedix Co., Ltd.
Fecha de decisión2024-07-10
Código de productoSBS
Comité asesorEN
DecisiónSubstantially Equivalent

Resumen del dispositivo

Lightin System, Lightin, Lightin Generator is the device name listed in this FDA 510(k) record. The listed applicant is Solmedix Co., Ltd.. It received FDA 510(k) clearance on 2024-07-10 under 510(k) number K232177. The device is classified under product code SBS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Lightin System, Lightin, Lightin Generator?

Lightin System, Lightin, Lightin Generator is a medical device that received FDA 510(k) clearance on 2024-07-10. The listed applicant is Solmedix Co., Ltd.. The 510(k) number is K232177.

When did Lightin System, Lightin, Lightin Generator receive FDA 510(k) clearance?

Lightin System, Lightin, Lightin Generator received FDA 510(k) clearance on 2024-07-10, under 510(k) number K232177.

Who is the listed applicant for Lightin System, Lightin, Lightin Generator?

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

What is the FDA product code for Lightin System, Lightin, Lightin Generator?

The FDA product code for Lightin System, Lightin, Lightin Generator is SBS.

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Fuente oficial

Ver en la base de datos de la FDA →

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