FDA 510(k)

PrimeSight UltraView System

N.º K: K253905 · 2026-04-07

Fecha de decisión2026-04-07

Código de productoFAJ

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

PrimeSight UltraView System is the device name listed in this FDA 510(k) record. The listed applicant is Cogentix Medical, Inc.. It received FDA 510(k) clearance on 2026-04-07 under 510(k) number K253905. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PrimeSight UltraView System?

PrimeSight UltraView System is a medical device that received FDA 510(k) clearance on 2026-04-07. The listed applicant is Cogentix Medical, Inc.. The 510(k) number is K253905.

When did PrimeSight UltraView System receive FDA 510(k) clearance?

PrimeSight UltraView System received FDA 510(k) clearance on 2026-04-07, under 510(k) number K253905.

Who is the listed applicant for PrimeSight UltraView System?

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

What is the FDA product code for PrimeSight UltraView System?

The FDA product code for PrimeSight UltraView System is FAJ.

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

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Fuente oficial

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