Inari Medical, Inc.

Inari Medical, Inc. — FDA 510(k) Submissions

Inari Medical, Inc. has submitted 30 FDA 510(k) premarket notifications since 2015, of which 30 received clearance as substantially equivalent to a predicate device.

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