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FDA 510(k)

Cleveland Multiport Ventricular Catheter Set

N.º K: K161731 · 2017-03-27

SolicitanteParker Hannifin Corp.
Fecha de decisión2017-03-27
Código de productoHCA
Comité asesorNE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Cleveland Multiport Ventricular Catheter Set is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corp.. It received FDA 510(k) clearance on 2017-03-27 under 510(k) number K161731. The device is classified under product code HCA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Cleveland Multiport Ventricular Catheter Set?

Cleveland Multiport Ventricular Catheter Set is a medical device that received FDA 510(k) clearance on 2017-03-27. The listed applicant is Parker Hannifin Corp.. The 510(k) number is K161731.

When did Cleveland Multiport Ventricular Catheter Set receive FDA 510(k) clearance?

Cleveland Multiport Ventricular Catheter Set received FDA 510(k) clearance on 2017-03-27, under 510(k) number K161731.

Who is the listed applicant for Cleveland Multiport Ventricular Catheter Set?

The FDA 510(k) record lists Parker Hannifin Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cleveland Multiport Ventricular Catheter Set?

The FDA product code for Cleveland Multiport Ventricular Catheter Set is HCA.

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Fuente oficial

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