FDA 510(k)

ViaValve Safety I.V. Catheter

N.º K: K160235 · 2016-06-30

Fecha de decisión2016-06-30

Código de productoFOZ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

ViaValve Safety I.V. Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Smiths Medical Asd, Inc.. It received FDA 510(k) clearance on 2016-06-30 under 510(k) number K160235. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ViaValve Safety I.V. Catheter?

ViaValve Safety I.V. Catheter is a medical device that received FDA 510(k) clearance on 2016-06-30. The listed applicant is Smiths Medical Asd, Inc.. The 510(k) number is K160235.

When did ViaValve Safety I.V. Catheter receive FDA 510(k) clearance?

ViaValve Safety I.V. Catheter received FDA 510(k) clearance on 2016-06-30, under 510(k) number K160235.

Who is the listed applicant for ViaValve Safety I.V. Catheter?

The FDA 510(k) record lists Smiths Medical Asd, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ViaValve Safety I.V. Catheter?

The FDA product code for ViaValve Safety I.V. Catheter is FOZ.

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Fuente oficial

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