Galvanize Therapeutics, Inc.

Galvanize Therapeutics, Inc. — FDA 510(k) Submissions

Galvanize Therapeutics, Inc. has submitted 2 FDA 510(k) premarket notifications since 2022, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Low Energy Direct Current Thermal Ablation System . Use the specialty filter in the sidebar to narrow results.