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
-
21 to 28 of 28 Results
ProductCode: OWB Applicant: SIEMENS MEDICAL SOLUTIONS USA, INC. Decision Date To: 02/04/2023
 < 
 1 
 2 
 3 
 
Results per Page
New Search  
Export all 28 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 q and q.zen- modular angiographic system SIEMENS MEDICAL SOLUTIONS USA, INC. K123529 02/26/2013
syngo aortic valveguide software SIEMENS MEDICAL SOLUTIONS USA, INC. K113027 11/22/2011
axiom luminos drf SIEMENS MEDICAL SOLUTIONS USA, INC. K062623 08/22/2007
axiom artis - modular angiographic system SIEMENS MEDICAL SOLUTIONS USA, INC. K052202 03/07/2006
u04 SIEMENS MEDICAL SOLUTIONS USA, INC. K010942 04/12/2001
urf digital - ot SIEMENS MEDICAL SOLUTIONS USA, INC. K992660 11/05/1999
siregragh t.o.p. 33 and siregraph t.o.p. 40 universal fluoroscopic x-ray systems SIEMENS MEDICAL SOLUTIONS USA, INC. K970734 04/21/1997
uroskop d1, uroskop d2, and uroskop d3 SIEMENS MEDICAL SOLUTIONS USA, INC. K923049 09/15/1992
-
-