Nexus Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nexus Medical, LLC - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Nexus Medical, LLC has 16 FDA 510(k) cleared general hospital devices. Based in Raleigh, US.
Historical record: 16 cleared submissions from 2003 to 2015.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nexus Medical, LLC
16 devices
Cleared
Jan 16, 2015
All Safe Huber Safety Infusion Set
General Hospital
123d
Cleared
May 22, 2014
NEXUS NIS-6P LUER ACTIVATED DEVICE
General Hospital
203d
Cleared
Jul 09, 2013
NEXUS IV TUBING SET WITH LUER-ACCESSBILE ONE-WAY CHECK VALVE - IV PLUS
General Hospital
102d
Cleared
Jun 12, 2013
NEXUS TKO-6P LUER ACTIVATED DEVICE
General Hospital
113d
Cleared
Apr 18, 2012
NEXUS TKO-6, LUER-ACTIVATED DEVICE
General Hospital
153d
Cleared
Apr 26, 2010
NEXUS PRESSURE RATED EXTENSION SETS
General Hospital
264d
Cleared
Mar 10, 2010
NEXUS INTRAVASCULAR TUBING SETS-PRE-PIERCED
General Hospital
169d
Cleared
Feb 04, 2010
NEXUS INJECTION SITE, MODEL NIS-8
General Hospital
170d
Cleared
Nov 14, 2008
NEXUS I.V. NEEDLESS ACCESS CANNULA FOR INTRAVASCULAR ADMINISTRATION SETS
General Hospital
207d
Cleared
Nov 10, 2008
NEXUS I.V. FLUID TRANSFER DEVICE
General Hospital
217d
Cleared
Dec 15, 2006
NEXUS IRRIGATION TUBING SET
Gastroenterology & Urology
107d
Cleared
Dec 08, 2005
NEXUSTKO NEEDLELESS ACCESS DEVICE, MODEL NIS-5
General Hospital
30d