Viramed Biotech AG

Viramed Biotech AG — FDA 510(k) Submissions

Viramed Biotech AG has submitted 7 FDA 510(k) premarket notifications since 2005, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reagent, Borrelia Serological Reagent . Use the specialty filter in the sidebar to narrow results.