FDA 510(k)

EPIQ Series Diagnostic Ultrasound System

N.º K: K260123 · 2026-05-27

Fecha de decisión2026-05-27

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

EPIQ Series Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, LLC. It received FDA 510(k) clearance on 2026-05-27 under 510(k) number K260123. 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 EPIQ Series Diagnostic Ultrasound System?

EPIQ Series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2026-05-27. The listed applicant is Philips Ultrasound, LLC. The 510(k) number is K260123.

When did EPIQ Series Diagnostic Ultrasound System receive FDA 510(k) clearance?

EPIQ Series Diagnostic Ultrasound System received FDA 510(k) clearance on 2026-05-27, under 510(k) number K260123.

Who is the listed applicant for EPIQ Series Diagnostic Ultrasound System?

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

What is the FDA product code for EPIQ Series Diagnostic Ultrasound System?

The FDA product code for EPIQ Series Diagnostic Ultrasound System is IYN.

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Otros registros que enlistan a Philips Ultrasound, LLC como solicitante

K262548EPIQ Inspira Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System K262311Sistema de Ultrasonido Diagnóstico de la Serie Alturion K261211Philips EPIQ Series Diagnostic Ultrasound System; Philips Affiniti Series Diagnostic Ultrasound System K260667Sistema de Ultrasonido Diagnóstico de la Serie Alturion K260680EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems K252558Lumify Diagnostic Ultrasound System

Ver todos los 27 dispositivos →

Dispositivos relacionados (Código: IYN)

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.