• 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: 01/25/2015
 < 
 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]
modification to ge discovery ls system GE MEDICAL SYSTEMS K040172 04/07/2004
modification to: lightspeed plus mobile ct system GE MEDICAL SYSTEMS K012836 09/07/2001
optima ct660 GE MEDICAL SYSTEMS, LLC K110227 07/20/2011
optima ct660 GE MEDICAL SYSTEMS, LLC K131576 08/30/2013
revolution apex, revolution apex elite, revolution apex plus, revolution apex select,revolution ct; revolution ct es; revolution ct with apex edition; revolution ct es with apex edition GE Medical Systems,LLC K213715 12/17/2021
revolution ct GE Medical Systems, L.L.C. K163213 12/16/2016
revolution ct GE MEDICAL SYSTEMS, LLC K133705 04/11/2014
revolution ct, revolution ct es, revolution apex, revolution ct with apex edition GE Medical Systems, LLC K191777 07/26/2019
smart breath respiratory compensation option GE MEDICAL SYSTEMS K022919 09/19/2002
smart vessel analysis (smart va) option GE MEDICAL SYSTEMS, INC. K993792 11/24/1999
-
-