510(k) K140270

NEXUS MIDLINE CT CATHETER by Health Line International Corporation — Product Code FOZ

K140270 is an FDA 510(k) premarket notification submitted by Health Line International Corporation for the device "NEXUS MIDLINE CT CATHETER". The FDA issued a decision of Substantially Equivalent on August 20, 2014. 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. Health Line International Corporation has at least 10 other 510(k) clearances on record.