FDA 510(k)

Vein Clamps, Artery Clamps

Número K: K161315 · 2016-08-18

RequerenteAros Surgical Instruments Corporation

Data da decisão2016-08-18

Código do produtoDXC

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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Fonte oficial

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