Reflow Medical, Inc.

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

Reflow Medical, Inc. has submitted 9 FDA 510(k) premarket notifications since 2016, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Percutaneous, Peripheral Temporary And Retrievable Stent System . Use the specialty filter in the sidebar to narrow results.