• 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 4 of 4 Results
ProductCode: DXE Applicant: VASCUTECH, INC. Decision Date To: 05/21/2024
Results per Page
New Search  
Export all 4 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]
lemaitre irrigation catheter VASCUTECH, INC. K992933 03/08/2000
lemaitre venous thrombectomy catheter VASCUTECH, INC. K992934 03/01/2000
lemaitre balloon catheter with irrigation VASCUTECH, INC. K992940 02/22/2000
lemaitre embolectomy catheter VASCUTECH, INC. K992368 12/09/1999
-
-