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FDA 510(k)

FlowArt® Needle-Free Split Septum Valve

N.º K: K222889 · 2023-01-20

SolicitanteAsset Medikal Tasarim San Tic As.
Fecha de decisión2023-01-20
Código de productoFPA
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

FlowArt® Needle-Free Split Septum Valve is the device name listed in this FDA 510(k) record. The listed applicant is Asset Medikal Tasarim San Tic As.. It received FDA 510(k) clearance on 2023-01-20 under 510(k) number K222889. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the FlowArt® Needle-Free Split Septum Valve?

FlowArt® Needle-Free Split Septum Valve is a medical device that received FDA 510(k) clearance on 2023-01-20. The listed applicant is Asset Medikal Tasarim San Tic As.. The 510(k) number is K222889.

When did FlowArt® Needle-Free Split Septum Valve receive FDA 510(k) clearance?

FlowArt® Needle-Free Split Septum Valve received FDA 510(k) clearance on 2023-01-20, under 510(k) number K222889.

Who is the listed applicant for FlowArt® Needle-Free Split Septum Valve?

The FDA 510(k) record lists Asset Medikal Tasarim San Tic As. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FlowArt® Needle-Free Split Septum Valve?

The FDA product code for FlowArt® Needle-Free Split Septum Valve is FPA.

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Dispositivos relacionados (Código: FPA)

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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