FDA 510(k)

Full Digital Colour Doppler Ultrasonic Diagnostic System

N.º K: K183041 · 2019-07-10

SolicitanteWuhan Zoncare Bio-medical Electronics Co., Ltd.

Fecha de decisión2019-07-10

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Full Digital Colour Doppler Ultrasonic Diagnostic System is the device name listed in this FDA 510(k) record. The listed applicant is Wuhan Zoncare Bio-medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K183041. 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 Full Digital Colour Doppler Ultrasonic Diagnostic System?

Full Digital Colour Doppler Ultrasonic Diagnostic System is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Wuhan Zoncare Bio-medical Electronics Co., Ltd.. The 510(k) number is K183041.

When did Full Digital Colour Doppler Ultrasonic Diagnostic System receive FDA 510(k) clearance?

Full Digital Colour Doppler Ultrasonic Diagnostic System received FDA 510(k) clearance on 2019-07-10, under 510(k) number K183041.

Who is the listed applicant for Full Digital Colour Doppler Ultrasonic Diagnostic System?

The FDA 510(k) record lists Wuhan Zoncare Bio-medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Full Digital Colour Doppler Ultrasonic Diagnostic System?

The FDA product code for Full Digital Colour Doppler Ultrasonic Diagnostic System is IYN.

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Dispositivos relacionados (Código: IYN)

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