Angiodynamics

Angiodynamics — FDA 510(k) Submissions

Angiodynamics has submitted 2 FDA 510(k) premarket notifications since 2014, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubing, Pump, Cardiopulmonary Bypass, Low Energy Direct Current Thermal Ablation System . Use the specialty filter in the sidebar to narrow results.