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 2 of 2 Results
ProductCode: FOZ Applicant: ETHICON ENDO-SURGERY, INC. Decision Date To: 05/29/2024
Results per Page
New Search  
Export all 2 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]
acuvance plus safety iv catheter, protectiv plus safety iv catheter, optiva iv catheter ETHICON ENDO-SURGERY, INC. K030571 03/28/2003
protectiv acuvance iv catheter system ETHICON ENDO-SURGERY, INC. K012128 08/01/2001
-
-