FDA 510(k)

NMI DUAL PORT II

N.º K: K151239 · 2016-06-06

Fecha de decisión2016-06-06

Código de productoLJT

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

NMI DUAL PORT II is the device name listed in this FDA 510(k) record. The listed applicant is Navilyst Medical, Inc.. It received FDA 510(k) clearance on 2016-06-06 under 510(k) number K151239. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the NMI DUAL PORT II?

NMI DUAL PORT II is a medical device that received FDA 510(k) clearance on 2016-06-06. The listed applicant is Navilyst Medical, Inc.. The 510(k) number is K151239.

When did NMI DUAL PORT II receive FDA 510(k) clearance?

NMI DUAL PORT II received FDA 510(k) clearance on 2016-06-06, under 510(k) number K151239.

Who is the listed applicant for NMI DUAL PORT II?

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

What is the FDA product code for NMI DUAL PORT II?

The FDA product code for NMI DUAL PORT II is LJT.

Otros registros que enlistan a Navilyst Medical, Inc. como solicitante

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Fuente oficial

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