Veridex, LLC is one of 14046 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Veridex, LLC - FDA 510(k) Cleared Devices
Recent clearances: CELLTRACKS ANALYZER II SYSTEM, CELLTRACKS AUTOPREP SYSTEM, CELLTRACKS AUTOPREP SYSTEM
12
Total
12
Cleared
0
Denied
Veridex, LLC has 12 FDA 510(k) cleared pathology devices. Based in Raritan, US.
Historical record: 12 cleared submissions from 2004 to 2013.
Browse the complete list of FDA 510(k) cleared pathology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Veridex, LLC
12 devices
Cleared
Jun 20, 2013
CELLTRACKS ANALYZER II SYSTEM
Pathology
90d
Cleared
Dec 13, 2012
CELLTRACKS AUTOPREP SYSTEM
Pathology
90d
Cleared
Jan 20, 2012
CELLTRACKS AUTOPREP SYSTEM
Pathology
340d
Cleared
Dec 12, 2011
CELLTRACKS ANALYER II
Pathology
45d
Cleared
Dec 21, 2010
CELLSEARCH CIRCULATING TUMOR CELL KIT MODEL 7900001
Pathology
22d
Cleared
Aug 26, 2010
CELLTRACKS AUTOPREP SYSTEM MODEL:9541
Hematology
169d
Cleared
Feb 26, 2008
CELLSEARCH CIRCULATING TUMOR CELL KIT
Pathology
90d
Cleared
Nov 20, 2007
CELLSEARCH CIRCULATING TUMOR CELL KIT
Pathology
148d
Cleared
Dec 14, 2006
CELLSEARCH CIRCULATING TUMOR CELL KIT
Pathology
150d
Cleared
Oct 27, 2005
MODIFICATION TO CELLSEARCH CIRCULATING TUMOR CELL KIT
Pathology
77d
Cleared
Mar 15, 2005
CELLSEARCH CIRCULATING TUMOR CELL KIT
Pathology
41d
Cleared
Jun 28, 2004
CELLSEARCH EPITHELIAL CELL CONTROL KIT
Hematology
83d