FDA 510(k)

Amecath Peripheral inserted Central Venous Catheter Sets

Número K: K152819 · 2016-02-05

Data da decisão2016-02-05

Código do produtoLJS

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Amecath Peripheral inserted Central Venous Catheter Sets is the device name listed in this FDA 510(k) record. The listed applicant is Ameco Medical Industries. It received FDA 510(k) clearance on 2016-02-05 under 510(k) number K152819. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Amecath Peripheral inserted Central Venous Catheter Sets?

Amecath Peripheral inserted Central Venous Catheter Sets is a medical device that received FDA 510(k) clearance on 2016-02-05. The listed applicant is Ameco Medical Industries. The 510(k) number is K152819.

When did Amecath Peripheral inserted Central Venous Catheter Sets receive FDA 510(k) clearance?

Amecath Peripheral inserted Central Venous Catheter Sets received FDA 510(k) clearance on 2016-02-05, under 510(k) number K152819.

Who is the listed applicant for Amecath Peripheral inserted Central Venous Catheter Sets?

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

What is the FDA product code for Amecath Peripheral inserted Central Venous Catheter Sets?

The FDA product code for Amecath Peripheral inserted Central Venous Catheter Sets is LJS.

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