Avenu Medical

Avenu Medical — FDA 510(k) Submissions

Avenu Medical has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Percutaneous Catheter For Creation Of An Arteriovenous Fistula For Hemodialysis Access . Use the specialty filter in the sidebar to narrow results.