Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector

K-Number: K170336 · 2017-03-10

Decision Date2017-03-10
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2017-03-10 under approval number K170336. 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 (Single Port) with MaxZero Needleless Connector?

BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector is a medical device that received FDA 510(k) clearance on 2017-03-10. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K170336.

When was BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector approved by the FDA?

BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector received FDA 510(k) clearance on 2017-03-10, under approval number K170336.

What company makes BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector?

BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector?

The FDA product code for BD Nexiva Closed IV Catheter System (Single Port) with MaxZero Needleless Connector is FOZ.

Related Clinical Trials

Related PubMed Literature

Other Devices by Becton, Dickinson and Company

View all 100 devices →

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.