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400um Perforator and Accessory Vein Ablation Kit

Page Type
Cleared 510(K)
510(k) Number
K181044
510(k) Type
Traditional
Applicant
AngioDynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2018
Days to Decision
77 days
Submission Type
Summary

400um Perforator and Accessory Vein Ablation Kit

Page Type
Cleared 510(K)
510(k) Number
K181044
510(k) Type
Traditional
Applicant
AngioDynamics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2018
Days to Decision
77 days
Submission Type
Summary