Last synced on 25 January 2026 at 3:41 am

AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081933
510(k) Type
Traditional
Applicant
Avalon Laboratories, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2008
Days to Decision
88 days
Submission Type
Summary

AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, 24FR, 26FR, 28FR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081933
510(k) Type
Traditional
Applicant
Avalon Laboratories, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2008
Days to Decision
88 days
Submission Type
Summary