Last synced on 25 January 2026 at 3:41 am

AngioVac C20, AngioVac C180

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190594
510(k) Type
Traditional
Applicant
AngioDynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
120 days
Submission Type
Summary

AngioVac C20, AngioVac C180

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190594
510(k) Type
Traditional
Applicant
AngioDynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
120 days
Submission Type
Summary