BD Nexiva Closed IV Catheter System
K-Number: K183399 · 2019-03-20
Device Summary
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.
Related Clinical Trials
Other Devices by Becton Dickinson Infusion Therapy Systems, Inc.
Related Devices (Code: FOZ)
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.