• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
1 to 10 of 10 Results
ProductCode: NQI Applicant: VERIDEX, LLC Decision Date To: 05/28/2024
Results per Page
New Search  
Export all 10 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
celltracks analyzer ii system VERIDEX, LLC K130794 06/20/2013
celltracks autoprep system VERIDEX, LLC K122821 12/13/2012
celltracks autoprep system VERIDEX, LLC K110406 01/20/2012
celltracks analyer ii VERIDEX, LLC K113181 12/12/2011
cellsearch circulating tumor cell kit model 7900001 VERIDEX, LLC K103502 12/21/2010
cellsearch circulating tumor cell kit VERIDEX, LLC K073338 02/26/2008
cellsearch circulating tumor cell kit VERIDEX, LLC K071729 11/20/2007
cellsearch circulating tumor cell kit VERIDEX, LLC K062013 12/14/2006
modification to cellsearch circulating tumor cell kit VERIDEX, LLC K052191 10/27/2005
cellsearch circulating tumor cell kit VERIDEX, LLC K050245 03/15/2005
-
-