FDA 510(k)

Perifix FX Catheter; Contiplex FX Catheter

N.º K: K231242 · 2023-09-15

Fecha de decisión2023-09-15

Código de productoBSO

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Perifix FX Catheter; Contiplex FX Catheter is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2023-09-15 under 510(k) number K231242. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Perifix FX Catheter; Contiplex FX Catheter?

Perifix FX Catheter; Contiplex FX Catheter is a medical device that received FDA 510(k) clearance on 2023-09-15. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K231242.

When did Perifix FX Catheter; Contiplex FX Catheter receive FDA 510(k) clearance?

Perifix FX Catheter; Contiplex FX Catheter received FDA 510(k) clearance on 2023-09-15, under 510(k) number K231242.

Who is the listed applicant for Perifix FX Catheter; Contiplex FX Catheter?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Perifix FX Catheter; Contiplex FX Catheter?

The FDA product code for Perifix FX Catheter; Contiplex FX Catheter is BSO.

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Fuente oficial

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