FDA 510(k)

BD Nexiva™ Closed IV Catheter System

K号: K243403 · 2025-07-25

申请人Becton Dickinson Infusion Therapy Systems, Inc.

决定日期2025-07-25

产品代码FOZ

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决定实质等同

器械摘要

BD Nexiva™ Closed IV Catheter System is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2025-07-25 under 510(k) number K243403. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Nexiva™ Closed IV Catheter System?

BD Nexiva™ Closed IV Catheter System is a medical device that received FDA 510(k) clearance on 2025-07-25. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K243403.

When did BD Nexiva™ Closed IV Catheter System receive FDA 510(k) clearance?

BD Nexiva™ Closed IV Catheter System received FDA 510(k) clearance on 2025-07-25, under 510(k) number K243403.

Who is the listed applicant for BD Nexiva™ Closed IV Catheter System?

The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Nexiva™ Closed IV Catheter System?

The FDA product code for BD Nexiva™ Closed IV Catheter System is FOZ.

列明Becton Dickinson Infusion Therapy Systems, 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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官方来源

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