FDA 510(k)

North-vision Multi-parameter Patient Monitor

N.º K: K173036 · 2018-12-21

Fecha de decisión2018-12-21

Código de productoMHX

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

North-vision Multi-parameter Patient Monitor is the device name listed in this FDA 510(k) record. The listed applicant is North-Vision Tech., Inc.. It received FDA 510(k) clearance on 2018-12-21 under 510(k) number K173036. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the North-vision Multi-parameter Patient Monitor?

North-vision Multi-parameter Patient Monitor is a medical device that received FDA 510(k) clearance on 2018-12-21. The listed applicant is North-Vision Tech., Inc.. The 510(k) number is K173036.

When did North-vision Multi-parameter Patient Monitor receive FDA 510(k) clearance?

North-vision Multi-parameter Patient Monitor received FDA 510(k) clearance on 2018-12-21, under 510(k) number K173036.

Who is the listed applicant for North-vision Multi-parameter Patient Monitor?

The FDA 510(k) record lists North-Vision Tech., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for North-vision Multi-parameter Patient Monitor?

The FDA product code for North-vision Multi-parameter Patient Monitor is MHX.

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Fuente oficial

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