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FDA 510(k)

Rubber Utility Catheter

K-Number: K251864 · 2026-02-23

ApplicantC.R. Bard, Inc.
Decision Date2026-02-23
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the Rubber Utility Catheter?

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

When was Rubber Utility Catheter approved by the FDA?

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

What company makes Rubber Utility Catheter?

Rubber Utility Catheter is manufactured by C.R. Bard, Inc..

What is the FDA product code for Rubber Utility Catheter?

The FDA product code for Rubber Utility Catheter is KOD.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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