FDA 510(k)

Rubber Utility Catheter

Número K: K251864 · 2026-02-23

Data da decisão2026-02-23

Código do produtoKOD

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Rubber Utility Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2026-02-23 under 510(k) number K251864. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Rubber Utility Catheter?

Rubber Utility Catheter is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K251864.

When did Rubber Utility Catheter receive FDA 510(k) clearance?

Rubber Utility Catheter received FDA 510(k) clearance on 2026-02-23, under 510(k) number K251864.

Who is the listed applicant for Rubber Utility Catheter?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Rubber Utility Catheter?

The FDA product code for Rubber Utility Catheter is KOD.

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