FDA 510(k)

Clivia series Diagnostic Ultrasound System

N.º K: K211886 · 2021-12-02

SolicitanteShenzhen Wisonic Medical Technology Co. , Ltd.

Fecha de decisión2021-12-02

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Clivia series Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Wisonic Medical Technology Co. , Ltd.. It received FDA 510(k) clearance on 2021-12-02 under 510(k) number K211886. 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 Clivia series Diagnostic Ultrasound System?

Clivia series Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2021-12-02. The listed applicant is Shenzhen Wisonic Medical Technology Co. , Ltd.. The 510(k) number is K211886.

When did Clivia series Diagnostic Ultrasound System receive FDA 510(k) clearance?

Clivia series Diagnostic Ultrasound System received FDA 510(k) clearance on 2021-12-02, under 510(k) number K211886.

Who is the listed applicant for Clivia series Diagnostic Ultrasound System?

The FDA 510(k) record lists Shenzhen Wisonic Medical Technology Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Clivia series Diagnostic Ultrasound System?

The FDA product code for Clivia series Diagnostic Ultrasound System is IYN.

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Otros registros que enlistan a Shenzhen Wisonic Medical Technology Co. , Ltd. como solicitante

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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.