FDA 510(k)

Vu-Path Ultrasound System

N.º K: K203657 · 2021-06-25

Fecha de decisión2021-06-25

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Vu-Path Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Crystalline Medical. It received FDA 510(k) clearance on 2021-06-25 under 510(k) number K203657. 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 Vu-Path Ultrasound System?

Vu-Path Ultrasound System is a medical device that received FDA 510(k) clearance on 2021-06-25. The listed applicant is Crystalline Medical. The 510(k) number is K203657.

When did Vu-Path Ultrasound System receive FDA 510(k) clearance?

Vu-Path Ultrasound System received FDA 510(k) clearance on 2021-06-25, under 510(k) number K203657.

Who is the listed applicant for Vu-Path Ultrasound System?

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

What is the FDA product code for Vu-Path Ultrasound System?

The FDA product code for Vu-Path Ultrasound System is IYN.

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Dispositivos relacionados (Código: IYN)

Fuente oficial

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