510(k) K172204

BD Intima II PLUS Closed IV Catheter System by Becton, Dickinson And Company — Product Code FOZ

K172204 is an FDA 510(k) premarket notification submitted by Becton, Dickinson And Company for the device "BD Intima II PLUS Closed IV Catheter System". The FDA issued a decision of Substantially Equivalent on Aug 17, 2017. The device falls under product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days), a Class II device regulated under 21 CFR 880.5200. Becton, Dickinson And Company has 329 other 510(k) clearances on record.