• 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
-
51 to 60 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 11/26/2014
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
Results per Page
New Search  
Export all 185 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]
miser contrast management system MERIT MEDICAL SYSTEMS, INC. K083576 12/23/2008
iv administration set U.S. SAFETY SYRINGES CO., INC. K080660 05/13/2008
novolet U.S. SAFETY SYRINGES CO., INC. K080665 05/13/2008
smartport ct mp port access system and lifeguard ct safety infusion set ANGIODYNAMICS, INC. K072375 12/13/2007
maxplus tru-swab positive displacement connector MEDEGEN MEDICAL MANUFACTURING SYSTEM K072542 09/25/2007
accu-chek ultraflex infusion set DISETRONIC MEDICAL SYSTEMS AG K070189 02/21/2007
vortex ct port access system and lifeguard safety infusion set RITA MEDICAL SYSTEMS, INC. K062414 02/01/2007
maxplus tru-swab positive displacement connector MEDEGEN MEDICAL MANUFACTURING SYSTEM K051939 08/01/2005
angiodynamics tumescent infusion device ANGIODYNAMICS, INC. K051142 07/13/2005
bd posiflow positive displacement valve BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. K050207 04/07/2005
-
-