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FDA 510(k)

Ventway Sparrow

N.º K: K202970 · 2021-01-29

SolicitanteInovytech Medical Solutions , Ltd.
Fecha de decisión2021-01-29
Código de productoCBK
Comité asesorAN
DecisiónSubstantially Equivalent

Resumen del dispositivo

Ventway Sparrow is the device name listed in this FDA 510(k) record. The listed applicant is Inovytech Medical Solutions , Ltd.. It received FDA 510(k) clearance on 2021-01-29 under 510(k) number K202970. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ventway Sparrow?

Ventway Sparrow is a medical device that received FDA 510(k) clearance on 2021-01-29. The listed applicant is Inovytech Medical Solutions , Ltd.. The 510(k) number is K202970.

When did Ventway Sparrow receive FDA 510(k) clearance?

Ventway Sparrow received FDA 510(k) clearance on 2021-01-29, under 510(k) number K202970.

Who is the listed applicant for Ventway Sparrow?

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

What is the FDA product code for Ventway Sparrow?

The FDA product code for Ventway Sparrow is CBK.

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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