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: JAK Applicant: GE MEDICAL SYSTEMS, INC. Decision Date To: 04/24/2024
 
 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]
ge lightspeed act fp16 GE MEDICAL SYSTEMS, INC. K091673 06/24/2009
ge lightspeed rt16 / lightspeed xtra v2 ct system (aka ge lightspeed rt16 / lightspeed xtra ct system GE MEDICAL SYSTEMS, INC. K082104 09/02/2008
ct colonography GE MEDICAL SYSTEMS, INC. K023943 05/06/2003
hispeed dual GE MEDICAL SYSTEMS, INC. K021491 05/22/2002
hispeed x/i smart gantry option GE MEDICAL SYSTEMS, INC. K012385 08/10/2001
ct colonography/navigator2 GE MEDICAL SYSTEMS, INC. K012313 08/07/2001
ge ct-pet system GE MEDICAL SYSTEMS, INC. K010641 03/30/2001
lightspeed 2.0ct scanner system GE MEDICAL SYSTEMS, INC. K000300 02/15/2000
ct/e computed tomography scannner system GE MEDICAL SYSTEMS, INC. K993645 12/21/1999
ct perfusion option GE MEDICAL SYSTEMS, INC. K993791 11/24/1999
-
-