Relievant Medsystems, Inc.

Relievant Medsystems, Inc. — FDA 510(k) Submissions

Relievant Medsystems, Inc. has submitted 4 FDA 510(k) premarket notifications since 2007, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Probe, Radiofrequency Lesion . Use the specialty filter in the sidebar to narrow results.