Baylis Medical Technologies, Inc.

Baylis Medical Technologies, Inc. — FDA 510(k) Submissions

Baylis Medical Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cable, Transducer And Electrode, Patient, (including Connector), Catheter For Crossing Total Occlusions, Electrosurgical, Cutting & Coagulation & Accessories . Use the specialty filter in the sidebar to narrow results.