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 5 of 5 Results
ProductCode: FPA Applicant: CODAN US CORP. Decision Date To: 05/20/2022
Results per Page
New Search  
Export all 5 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]
i.v. set-luer lock with latex free injection site, model b411 CODAN US CORP. K001872 09/07/2000
codan us i.v. administration set, model b400 sp CODAN US CORP. K013714 03/28/2002
extension set light-safe, model bc565 CODAN US CORP. K021480 06/27/2002
iv administration and connect sets CODAN US CORP. K033301 03/04/2004
iv administration set b400 sp CODAN US CORP. K042693 10/21/2004
-
-