Nexus Medical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
16
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142590All Safe Huber Safety Infusion SetJanuary 16, 2015
K133351NEXUS NIS-6P LUER ACTIVATED DEVICEMay 22, 2014
K130879NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUSJuly 9, 2013
K130416NEXUS TKO-6P LUER ACTIVATED DEVICEJune 12, 2013
K113398NEXUS TKO-6, LUER-ACTIVATED DEVICEApril 18, 2012
K092382NEXUS PRESSURE RATED EXTENSION SETSApril 26, 2010
K092930NEXUS INTRAVASCULAR TUBING SETS-PRE-PIERCEDMarch 10, 2010
K092527NEXUS INJECTION SITE, MODEL NIS-8February 4, 2010
K081123NEXUS I.V. NEEDLESS ACCESS CANNULA FOR INTRAVASCULAR ADMINISTRATION SETSNovember 14, 2008
K080976NEXUS I.V. FLUID TRANSFER DEVICENovember 10, 2008
K062551NEXUS IRRIGATION TUBING SETDecember 15, 2006
K053129NEXUSTKO NEEDLELESS ACCESS DEVICE, MODEL NIS-5December 8, 2005
K041861NEXUS INTRAVENOUS TUBING SETS (NIVTS)November 26, 2004
K041844ALL SAFE HUBER SAFETY INFUSION SETSSeptember 3, 2004
K041845NEXUS PAV LUER LOCK DEVICE, MODEL NIS-4August 24, 2004
K024363NEXUS INJECTION SITE (NIS), MODEL NIS-1February 19, 2003