FDA 510(k)

Venture 0.014 Catheter

N.º K: K182570 · 2019-03-13

Fecha de decisión2019-03-13

Código de productoDQY

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Venture 0.014 Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, LLC. It received FDA 510(k) clearance on 2019-03-13 under 510(k) number K182570. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Venture 0.014 Catheter?

Venture 0.014 Catheter is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Vascular Solutions, LLC. The 510(k) number is K182570.

When did Venture 0.014 Catheter receive FDA 510(k) clearance?

Venture 0.014 Catheter received FDA 510(k) clearance on 2019-03-13, under 510(k) number K182570.

Who is the listed applicant for Venture 0.014 Catheter?

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

What is the FDA product code for Venture 0.014 Catheter?

The FDA product code for Venture 0.014 Catheter is DQY.

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Fuente oficial

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