510(k) K041845

NEXUS PAV LUER LOCK DEVICE, MODEL NIS-4 by Nexus Medical, LLC — Product Code FPA

K041845 is an FDA 510(k) premarket notification submitted by Nexus Medical, LLC for the device "NEXUS PAV LUER LOCK DEVICE, MODEL NIS-4". The FDA issued a decision of Substantially Equivalent on August 24, 2004. 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.