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
-
71 to 80 of 88 Results
ProductCode: JAK Applicant: GE MEDICAL SYSTEMS Decision Date To: 08/28/2016
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 > 
Results per Page
New Search  
Export all 88 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]
ct cord iq option 1.0 GE MEDICAL SYSTEMS K003408 11/17/2000
ct colonography/navigator2 GE MEDICAL SYSTEMS, INC. K012313 08/07/2001
ct colonography GE MEDICAL SYSTEMS, INC. K023943 05/06/2003
computed tomography x-ray system GE MEDICAL SYSTEMS K970606 04/04/1997
cardiq xpress 2.0 with snapshot freeze option cardiq xpress 2.0 reveal GE MEDICAL SYSTEMS SCS K120910 06/18/2012
cardiq suite GE Medical Systems SCS K213725 03/11/2022
cardiq function xpress GE MEDICAL SYSTEMS SCS K073153 02/26/2008
cardiq function GE MEDICAL SYSTEMS K013422 10/30/2001
cardiq express version 2.0 GE MEDICAL SYSTEMS K073138 02/26/2008
card iq analysis ii GE MEDICAL SYSTEMS K020796 03/26/2002
-
-