510(k) K142590

All Safe Huber Safety Infusion Set by Nexus Medical, LLC — Product Code FPA

K142590 is an FDA 510(k) premarket notification submitted by Nexus Medical, LLC for the device "All Safe Huber Safety Infusion Set". The FDA issued a decision of Substantially Equivalent on January 16, 2015. 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.