BD Nexiva Diffusics Closed IV Catheter Systems
K-Number: K173354 · 2017-12-15
Device Summary
Frequently Asked Questions
What is the BD Nexiva Diffusics Closed IV Catheter Systems?
BD Nexiva Diffusics Closed IV Catheter Systems is a medical device that received FDA 510(k) clearance on 2017-12-15. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K173354.
When did BD Nexiva Diffusics Closed IV Catheter Systems receive FDA 510(k) clearance?
BD Nexiva Diffusics Closed IV Catheter Systems received FDA 510(k) clearance on 2017-12-15, under 510(k) number K173354.
Who is the listed applicant for BD Nexiva Diffusics Closed IV Catheter Systems?
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 Diffusics Closed IV Catheter Systems?
The FDA product code for BD Nexiva Diffusics Closed IV Catheter Systems is FOZ.
Other records listing Becton Dickinson Infusion Therapy Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FOZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.