• 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 8 of 8 Results
ProductCode: FOZ Applicant: VYGON CORP. Decision Date To: 05/24/2024
Results per Page
New Search  
Export all 8 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: latex-free bionector, model# 896.019, 896.039 VYGON CORP. K070705 11/30/2007
multicath expert VYGON CORP. K061250 09/29/2006
vygon leader-flex VYGON CORP. K052564 04/05/2006
vygon latex free bionector VYGON CORP. K052881 03/02/2006
vygon umbilical cathether insertion tray VYGON CORP. K963196 09/09/1997
vygon lifevac mid-line tray VYGON CORP. K954112 05/09/1996
bionector VYGON CORP. K941678 06/26/1995
multicath placement kit VYGON CORP. K901640 08/10/1990
-
-