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 6 of 6 Results
ProductCode: OWB Applicant: GE MEDICAL SYSTEMS, INC. Decision Date To: 05/30/2023
Results per Page
New Search  
Export all 6 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 4100, innova 3100 GE MEDICAL SYSTEMS, INC. K042053 08/26/2004
digital fluoroscopic imaging system, model innova 4100 with tilt table option GE MEDICAL SYSTEMS, INC. K033244 10/16/2003
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
lcv+ version 2 GE MEDICAL SYSTEMS, INC. K993037 02/14/2000
-
-