Inari Medical

Inari Medical — FDA 510(k) Submissions

Inari Medical has submitted 26 FDA 510(k) premarket notifications since 2015, of which 26 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Peripheral Mechanical Thrombectomy With Aspiration, Apparatus, Autotransfusion, Catheter, Percutaneous . Use the specialty filter in the sidebar to narrow results.