BD Angiocath IV Catheter, BD Insyte IV Catheter

About This 510(k) Submission

K151698 is an FDA 510(k) clearance for the BD Angiocath IV Catheter, BD Insyte IV Catheter, 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 July 27, 2015, 33 days after receiving the submission on June 24, 2015. This device falls under the General Hospital review panel. Regulated under 21 CFR 880.5200.