FDA 510(k)

ViziShot 2 FLEX

N.º K: K163469 · 2017-04-06

SolicitanteOlympus Surgical Technologies America

Fecha de decisión2017-04-06

Código de productoKTI

Comité asesorEN

DecisiónSubstantially Equivalent

Resumen del dispositivo

ViziShot 2 FLEX is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Surgical Technologies America. It received FDA 510(k) clearance on 2017-04-06 under 510(k) number K163469. The device is classified under product code KTI. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ViziShot 2 FLEX?

ViziShot 2 FLEX is a medical device that received FDA 510(k) clearance on 2017-04-06. The listed applicant is Olympus Surgical Technologies America. The 510(k) number is K163469.

When did ViziShot 2 FLEX receive FDA 510(k) clearance?

ViziShot 2 FLEX received FDA 510(k) clearance on 2017-04-06, under 510(k) number K163469.

Who is the listed applicant for ViziShot 2 FLEX?

The FDA 510(k) record lists Olympus Surgical Technologies America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ViziShot 2 FLEX?

The FDA product code for ViziShot 2 FLEX is KTI.

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Fuente oficial

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