Nexiva? Closed IV Catheter System with NearPort? IV Access

About This 510(k) Submission

K231239 is an FDA 510(k) clearance for the Nexiva? Closed IV Catheter System with NearPort? IV Access, 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 September 22, 2023, 147 days after receiving the submission on April 28, 2023. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5200.