FDA 510(k)

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector

K-Number: K233529 · 2023-12-01

ApplicantBecton Dickinson Infusion Therapy Systems, Inc.

Decision Date2023-12-01

Product CodeFOZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector is a medical device manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2023-12-01 under approval number K233529. 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 System with BD MaxZero Needle-free Connector?

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector is a medical device that received FDA 510(k) clearance on 2023-12-01. It is manufactured by Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K233529.

When was BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector approved by the FDA?

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector received FDA 510(k) clearance on 2023-12-01, under approval number K233529.

What company makes BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector?

BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector is manufactured by Becton Dickinson Infusion Therapy Systems, Inc..

What is the FDA product code for BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector?

The FDA product code for BD Nexiva Diffusics Closed IV Catheter System with BD MaxZero Needle-free Connector is FOZ.

Related Clinical Trials

NCT07475091 Standardizing Swallow Pressure Measurements NOT_YET_RECRUITING NCT02193425 Reliability of the Human Brain Connectome COMPLETED NCT06510556 Feasibility Study of the FARAFLEX Mapping and PFA System RECRUITING NCT06958731 In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial ENROLLING_BY_INVITATION NCT06735534 Repeat Ablation of Persistent Atrial Fibrillation, Including Mitral Isthmus Catheter Ablation, With the FARAPULSE Pulsed Field Ablation System RECRUITING NCT07430293 Hybrid Closed-Loop Insulin Delivery After Pancreatectomy RECRUITING

Other Devices by Becton Dickinson Infusion Therapy Systems, Inc.

K161777BD Nexiva and BD Nexiva Diffusics Closed IV Catheter Systems K173354BD Nexiva Diffusics Closed IV Catheter Systems K183399BD Nexiva Closed IV Catheter System K201717BD Cathena Safety IV Catheter K192493BD Cathena (TM) Safety IV Catheter K220584BD Cathena Safety IV Catheter

View all 16 devices →

Related Devices (Code: FOZ)

K162894AccuCath Intravascular CatheterC.R. Bard, Inc. K161779MedSource TrueSafe Safety IV Catheter, MedSource TrueSafe Comfort Safety IV CatheterMedsource International, LLC K162377PowerGlide Pro Midline CatheterC.R. Bard, Inc. K161866BioFlo Midline CatheterNavilyst Medical, Inc. K161777BD Nexiva and BD Nexiva Diffusics Closed IV Catheter SystemsBecton Dickinson Infusion Therapy Systems, Inc. K160592SUPERCATH 6Togo Medikit Co., Ltd.

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.