Last synced on 20 June 2025 at 11:06 pm

AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081820
510(k) Type
Traditional
Applicant
AVALON LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2008
Days to Decision
101 days
Submission Type
Summary

AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081820
510(k) Type
Traditional
Applicant
AVALON LABORATORIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2008
Days to Decision
101 days
Submission Type
Summary