FDA 510(k)

Ventripoint Medical System Plus (VMS+)

N.º K: K173810 · 2018-05-14

SolicitanteVentripoint Diagnostics , Ltd.

Fecha de decisión2018-05-14

Código de productoIYN

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Ventripoint Medical System Plus (VMS+) is the device name listed in this FDA 510(k) record. The listed applicant is Ventripoint Diagnostics , Ltd.. It received FDA 510(k) clearance on 2018-05-14 under 510(k) number K173810. 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 Ventripoint Medical System Plus (VMS+)?

Ventripoint Medical System Plus (VMS+) is a medical device that received FDA 510(k) clearance on 2018-05-14. The listed applicant is Ventripoint Diagnostics , Ltd.. The 510(k) number is K173810.

When did Ventripoint Medical System Plus (VMS+) receive FDA 510(k) clearance?

Ventripoint Medical System Plus (VMS+) received FDA 510(k) clearance on 2018-05-14, under 510(k) number K173810.

Who is the listed applicant for Ventripoint Medical System Plus (VMS+)?

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

What is the FDA product code for Ventripoint Medical System Plus (VMS+)?

The FDA product code for Ventripoint Medical System Plus (VMS+) is IYN.

Ensayos clínicos relacionados

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Otros registros que enlistan a Ventripoint Diagnostics , Ltd. como solicitante

K241222Ventripoint Medical System Plus (VMS+) 4.0 K191493Ventripoint Medical System Plus (VMS+) 3.0

Dispositivos relacionados (Código: IYN)

Fuente oficial

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