FDA 510(k)

Pinzas Bipolares Fenestradas ArtiSential

N.º K: K190909 · 2020-02-13

Fecha de decisión2020-02-13

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

ArtiSential Bipolar Fenestrated Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Livsmed, Inc.. It received FDA 510(k) clearance on 2020-02-13 under 510(k) number K190909. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ArtiSential Bipolar Fenestrated Forceps?

ArtiSential Bipolar Fenestrated Forceps is a medical device that received FDA 510(k) clearance on 2020-02-13. The listed applicant is Livsmed, Inc.. The 510(k) number is K190909.

When did ArtiSential Bipolar Fenestrated Forceps receive FDA 510(k) clearance?

ArtiSential Bipolar Fenestrated Forceps received FDA 510(k) clearance on 2020-02-13, under 510(k) number K190909.

Who is the listed applicant for ArtiSential Bipolar Fenestrated Forceps?

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

What is the FDA product code for ArtiSential Bipolar Fenestrated Forceps?

The FDA product code for ArtiSential Bipolar Fenestrated Forceps is GEI.

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Fuente oficial

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