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FDA 510(k)

Electrosurgical Generator and Accessories

N.º K: K201224 · 2020-09-18

SolicitanteMedrange
Fecha de decisión2020-09-18
Código de productoGEI
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

Electrosurgical Generator and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is Medrange. It received FDA 510(k) clearance on 2020-09-18 under 510(k) number K201224. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Electrosurgical Generator and Accessories?

Electrosurgical Generator and Accessories is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Medrange. The 510(k) number is K201224.

When did Electrosurgical Generator and Accessories receive FDA 510(k) clearance?

Electrosurgical Generator and Accessories received FDA 510(k) clearance on 2020-09-18, under 510(k) number K201224.

Who is the listed applicant for Electrosurgical Generator and Accessories?

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

What is the FDA product code for Electrosurgical Generator and Accessories?

The FDA product code for Electrosurgical Generator and Accessories is GEI.

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Dispositivos relacionados (Código: GEI)

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Fuente oficial

Ver en la base de datos de la FDA →

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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