LimFlow, Inc.

LimFlow, Inc. — FDA 510(k) Submissions

LimFlow, 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 Device, Percutaneous Retrieval, Catheter For Crossing Total Occlusions, Valvulotome . Use the specialty filter in the sidebar to narrow results.