FDA 510(k)

Vein Clamps, Artery Clamps

N.º K: K161315 · 2016-08-18

SolicitanteAros Surgical Instruments Corporation

Fecha de decisión2016-08-18

Código de productoDXC

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Vein Clamps, Artery Clamps is the device name listed in this FDA 510(k) record. The listed applicant is Aros Surgical Instruments Corporation. It received FDA 510(k) clearance on 2016-08-18 under 510(k) number K161315. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Vein Clamps, Artery Clamps?

Vein Clamps, Artery Clamps is a medical device that received FDA 510(k) clearance on 2016-08-18. The listed applicant is Aros Surgical Instruments Corporation. The 510(k) number is K161315.

When did Vein Clamps, Artery Clamps receive FDA 510(k) clearance?

Vein Clamps, Artery Clamps received FDA 510(k) clearance on 2016-08-18, under 510(k) number K161315.

Who is the listed applicant for Vein Clamps, Artery Clamps?

The FDA 510(k) record lists Aros Surgical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vein Clamps, Artery Clamps?

The FDA product code for Vein Clamps, Artery Clamps is DXC.

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Fuente oficial

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