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FDA 510(k)

BD Nexiva Diffusics Closed IV Catheter Systems

K-Number: K173354 · 2017-12-15

Decision Date2017-12-15
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Nexiva Diffusics Closed IV Catheter Systems is a medical device manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2017-12-15 under approval number K173354. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K173354.

When was BD Nexiva Diffusics Closed IV Catheter Systems approved by the FDA?

BD Nexiva Diffusics Closed IV Catheter Systems received FDA 510(k) clearance on 2017-12-15, under approval number K173354.

What company makes BD Nexiva Diffusics Closed IV Catheter Systems?

BD Nexiva Diffusics Closed IV Catheter Systems is manufactured by Becton Dickinson Infusion Therapy Systems, Inc..

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.

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Official Source

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