Epimed International

Epimed International — FDA 510(k) Submissions

Epimed International has submitted 2 FDA 510(k) premarket notifications since 2008, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Conduction, Anesthetic (w/wo Introducer), Generator, Lesion, Radiofrequency . Use the specialty filter in the sidebar to narrow results.