Catheter Research C/O Burditt, Bowles & Radzius

Catheter Research C/O Burditt, Bowles & Radzius — FDA 510(k) Submissions

Catheter Research C/O Burditt, Bowles & Radzius has submitted 8 FDA 510(k) premarket notifications since 1987, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Steerable, System, Catheter Control, Steerable, Catheter, Intravascular, Diagnostic, Clip, Vascular . Use the specialty filter in the sidebar to narrow results.