510(k) K130879

NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS by Nexus Medical, LLC — Product Code FPA

K130879 is an FDA 510(k) premarket notification submitted by Nexus Medical, LLC for the device "NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS". The FDA issued a decision of Substantially Equivalent on July 9, 2013. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Nexus Medical, LLC has at least 10 other 510(k) clearances on record.