Neuravi Limited

Neuravi Limited — FDA 510(k) Submissions

Neuravi Limited has submitted 3 FDA 510(k) premarket notifications since 2021, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Percutaneous, Neurovasculature, Catheter, Thrombus Retriever . Use the specialty filter in the sidebar to narrow results.