• 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 21 Results
ProductCode: JAA Applicant: SIEMENS MEDICAL SOLUTIONS USA, INC Decision Date To: 07/28/2014
 
 1 
 2 
 3 
 > 
Results per Page
New Search
Export all 21 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]
artis one siemens medical solutions usa, inc. K133580 04/28/2014
artis q and q.zen- modular angiographic siemens medical solutions usa, inc. K123529 02/26/2013
syngo aortic valveguide software siemens medical solutions usa, inc. K113027 11/22/2011
luminos agile siemens medical solutions usa, inc. K111292 06/03/2011
uroskop omnia siemens medical solutions usa, inc. K101491 06/30/2010
axiom luminos drf siemens medical solutions usa, inc. K062623 08/22/2007
axiom artis - modular angiographic syste siemens medical solutions usa, inc. K052202 03/07/2006
siremobile c06 siemens medical solutions usa, inc. K040066 02/12/2004
modular angiography system axiom artis siemens medical solutions usa, inc. K021021 06/06/2002
u04 siemens medical solutions usa, inc. K010942 04/12/2001
-
-