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FDA 510(k)

BD Nexiva Closed IV Catheter System

K-Number: K183399 · 2019-03-20

Decision Date2019-03-20
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Nexiva Closed IV Catheter System is a medical device manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2019-03-20 under approval number K183399. 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 Closed IV Catheter System?

BD Nexiva Closed IV Catheter System is a medical device that received FDA 510(k) clearance on 2019-03-20. It is manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K183399.

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

BD Nexiva Closed IV Catheter System received FDA 510(k) clearance on 2019-03-20, under approval number K183399.

What company makes BD Nexiva Closed IV Catheter System?

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

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.

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Official Source

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