• 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: GEI Applicant: VIVANT MEDICAL, INC. Decision Date To: 03/28/2024
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]
loop microwave ablation probe VIVANT MEDICAL, INC. K023311 04/09/2003
tri-loop microwave ablation probe VIVANT MEDICAL, INC. K032047 08/06/2003
vivaring microwave ablation probe VIVANT MEDICAL, INC. K040279 03/02/2004
vivatip microwave ablation probe VIVANT MEDICAL, INC. K032702 10/03/2003
vivawave microwave ablation system, coaxial introducer VIVANT MEDICAL, INC. K050223 02/24/2005
vivawave microwave system VIVANT MEDICAL, INC. K011676 06/18/2002
-
-