FDA 510(k)

橡胶通用导管

K号: K251864 · 2026-02-23

决定日期2026-02-23

产品代码KOD

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决定实质等同

器械摘要

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.

常见问题

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.

列明C.R. Bard, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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