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
-
31 to 40 of 88 Results
ProductCode: JAK Applicant: GE MEDICAL SYSTEMS Decision Date To: 11/30/2015
 < 
 1 
 2 
 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]
discovery ct750 hd GE MEDICAL SYSTEMS, LLC K120833 06/12/2012
optima ct660 GE MEDICAL SYSTEMS, LLC K110227 07/20/2011
discovery model ct590 rt and optima model ct580 ct systems GE MEDICAL SYSTEMS, LLC K093581 04/19/2011
discovery model nm/ct 670 GE MEDICAL SYSTEMS F.I. HAIFA K093514 12/10/2009
ge lightspeed act fp16 GE MEDICAL SYSTEMS, INC. K091673 06/24/2009
ge xtreme injector option GE MEDICAL SYSTEMS, LLC K082960 10/17/2008
ge brightspeed delight ct scanner system GE MEDICAL SYSTEMS, LLC K082816 10/08/2008
ge lightspeed 7.2 ct scanner system GE MEDICAL SYSTEMS, LLC K082761 10/08/2008
ge lightspeed rt16 / lightspeed xtra v2 ct system (aka ge lightspeed rt16 / lightspeed xtra ct system GE MEDICAL SYSTEMS, INC. K082104 09/02/2008
cardiq express version 2.0 GE MEDICAL SYSTEMS K073138 02/26/2008
-
-