FDA 510(k)

Mais Central Venous Catheter

N.º K: K221827 · 2023-06-23

SolicitanteSaudi Mais Co. For Medical Products

Fecha de decisión2023-06-23

Código de productoFOZ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Mais Central Venous Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Saudi Mais Co. For Medical Products. It received FDA 510(k) clearance on 2023-06-23 under 510(k) number K221827. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Mais Central Venous Catheter?

Mais Central Venous Catheter is a medical device that received FDA 510(k) clearance on 2023-06-23. The listed applicant is Saudi Mais Co. For Medical Products. The 510(k) number is K221827.

When did Mais Central Venous Catheter receive FDA 510(k) clearance?

Mais Central Venous Catheter received FDA 510(k) clearance on 2023-06-23, under 510(k) number K221827.

Who is the listed applicant for Mais Central Venous Catheter?

The FDA 510(k) record lists Saudi Mais Co. For Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Mais Central Venous Catheter?

The FDA product code for Mais Central Venous Catheter is FOZ.

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Fuente oficial

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