• 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
-
11 to 18 of 18 Results
ProductCode: JAA Applicant: GE MEDICAL SYSTEMS Decision Date To: 07/24/2014
 < 
 1 
 2 
 
Results per Page
New Search  
Export all 18 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]
innova 3100 GE MEDICAL SYSTEMS K031637 08/22/2003
innova 2000 and innova 2000s (mobile version) GE MEDICAL SYSTEMS, INC. K024200 01/16/2003
innova 4100 GE MEDICAL SYSTEMS, INC. K023178 11/26/2002
innova and innova 2000 s GE MEDICAL SYSTEMS, INC. K022322 10/08/2002
expedio 500d r&f x-ray system GE MEDICAL SYSTEMS K011624 06/08/2001
lcv+ version 2 GE MEDICAL SYSTEMS, INC. K993037 02/14/2000
legend crf fluoro and rad system GE MEDICAL SYSTEMS, INC. K993665 11/12/1999
tc+ system (tilting c-arm system) GE MEDICAL SYSTEMS K936180 03/16/1994
-
-