FDA 510(k)

lntravascular Administration Sets with Stopcock and Manifold

Número K: K223175 · 2023-03-10

Data da decisão2023-03-10

Código do produtoFMG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

lntravascular Administration Sets with Stopcock and Manifold is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2023-03-10 under 510(k) number K223175. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the lntravascular Administration Sets with Stopcock and Manifold?

lntravascular Administration Sets with Stopcock and Manifold is a medical device that received FDA 510(k) clearance on 2023-03-10. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K223175.

When did lntravascular Administration Sets with Stopcock and Manifold receive FDA 510(k) clearance?

lntravascular Administration Sets with Stopcock and Manifold received FDA 510(k) clearance on 2023-03-10, under 510(k) number K223175.

Who is the listed applicant for lntravascular Administration Sets with Stopcock and Manifold?

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

What is the FDA product code for lntravascular Administration Sets with Stopcock and Manifold?

The FDA product code for lntravascular Administration Sets with Stopcock and Manifold is FMG.

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Fonte oficial

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