Cardio Flow Inc.,

Cardio Flow Inc., — FDA 510(k) Submissions

Cardio Flow Inc., has submitted 5 FDA 510(k) premarket notifications since 2022, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Peripheral, Atherectomy, Wire, Guide, Catheter . Use the specialty filter in the sidebar to narrow results.