Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 13 Results
ProductCode: GEX Applicant: VASCULAR SOLUTIONS, INC Decision Date To: 08/31/2015
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 13 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]
vari-lase wirefiber laser fiber VASCULAR SOLUTIONS, INC. K113140 12/22/2011
vari-lase endovenous laser console VASCULAR SOLUTIONS, INC. K093502 01/07/2010
vari-lase platinum bright tip laser fiber VASCULAR SOLUTIONS, INC. K091551 06/19/2009
vari-lase endovenous laser console, model 7542 VASCULAR SOLUTIONS, INC. K080104 03/26/2008
vari-lase wire fiber VASCULAR SOLUTIONS, INC. K072332 01/10/2008
vari-lase bright tip fiber VASCULAR SOLUTIONS, INC. K070216 03/16/2007
vari-lase endovenous laser console, model 7500 VASCULAR SOLUTIONS, INC. K062822 11/21/2006
vari-lase endovenous laser procedure kit VASCULAR SOLUTIONS, INC. K051287 07/29/2005
vascular solutions vari-lase endovenous laser procedure kit VASCULAR SOLUTIONS, INC. K050021 03/18/2005
vascular solutions vari-lase endovenous laser console VASCULAR SOLUTIONS, INC. K033237 11/20/2003
-
-