FDA 510(k)

EzVu Visual Vasopressor injector (EV-19)

N.º K: K241595 · 2025-02-27

SolicitanteVeol Medical Technologies Pvt , Ltd.

Fecha de decisión2025-02-27

Código de productoFBK

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

EzVu Visual Vasopressor injector (EV-19) is the device name listed in this FDA 510(k) record. The listed applicant is Veol Medical Technologies Pvt , Ltd.. It received FDA 510(k) clearance on 2025-02-27 under 510(k) number K241595. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the EzVu Visual Vasopressor injector (EV-19)?

EzVu Visual Vasopressor injector (EV-19) is a medical device that received FDA 510(k) clearance on 2025-02-27. The listed applicant is Veol Medical Technologies Pvt , Ltd.. The 510(k) number is K241595.

When did EzVu Visual Vasopressor injector (EV-19) receive FDA 510(k) clearance?

EzVu Visual Vasopressor injector (EV-19) received FDA 510(k) clearance on 2025-02-27, under 510(k) number K241595.

Who is the listed applicant for EzVu Visual Vasopressor injector (EV-19)?

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

What is the FDA product code for EzVu Visual Vasopressor injector (EV-19)?

The FDA product code for EzVu Visual Vasopressor injector (EV-19) is FBK.

Ensayos clínicos relacionados

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Otros registros que enlistan a Veol Medical Technologies Pvt , Ltd. como solicitante

K240205Ez Catch Auto; Ez Catch YR; Ez Catch TR

Dispositivos relacionados (Código: FBK)

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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.