FDA 510(k)

UltraVision 2 Diagnostic Ultrasound System

N.º K: K173265 · 2017-11-07

Fecha de decisión2017-11-07

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

UltraVision 2 Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Winprobe Corporation. It received FDA 510(k) clearance on 2017-11-07 under 510(k) number K173265. 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 UltraVision 2 Diagnostic Ultrasound System?

UltraVision 2 Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2017-11-07. The listed applicant is Winprobe Corporation. The 510(k) number is K173265.

When did UltraVision 2 Diagnostic Ultrasound System receive FDA 510(k) clearance?

UltraVision 2 Diagnostic Ultrasound System received FDA 510(k) clearance on 2017-11-07, under 510(k) number K173265.

Who is the listed applicant for UltraVision 2 Diagnostic Ultrasound System?

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

What is the FDA product code for UltraVision 2 Diagnostic Ultrasound System?

The FDA product code for UltraVision 2 Diagnostic Ultrasound System is IYN.

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Dispositivos relacionados (Código: IYN)

Fuente oficial

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