FDA 510(k)

Voluson Expert 18; Voluson Expert 20; Voluson Expert 22

N.º K: K242168 · 2024-12-20

SolicitanteGE Medical Systems Ultrasound and Primary Care Diagnostics

Fecha de decisión2024-12-20

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. It received FDA 510(k) clearance on 2024-12-20 under 510(k) number K242168. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Voluson Expert 18; Voluson Expert 20; Voluson Expert 22?

Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 is a medical device that received FDA 510(k) clearance on 2024-12-20. The listed applicant is GE Medical Systems Ultrasound and Primary Care Diagnostics. The 510(k) number is K242168.

When did Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 receive FDA 510(k) clearance?

Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 received FDA 510(k) clearance on 2024-12-20, under 510(k) number K242168.

Who is the listed applicant for Voluson Expert 18; Voluson Expert 20; Voluson Expert 22?

The FDA 510(k) record lists GE Medical Systems Ultrasound and Primary Care Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Voluson Expert 18; Voluson Expert 20; Voluson Expert 22?

The FDA product code for Voluson Expert 18; Voluson Expert 20; Voluson Expert 22 is IYN.

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Dispositivos relacionados (Código: IYN)

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.