BD Nexiva Diffusics Closed IV Catheter Systems

About This 510(k) Submission

K173354 is an FDA 510(k) clearance for the BD Nexiva Diffusics Closed IV Catheter Systems, a Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days (Class II — Special Controls, product code FOZ), submitted by Becton Dickinson Infusion Therapy Systems, Inc. (Sandy, US). The FDA issued a Cleared decision on December 15, 2017, 51 days after receiving the submission on October 25, 2017. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5200.