Hardy Media

Hardy Media — FDA 510(k) Submissions

Hardy Media has submitted 114 FDA 510(k) premarket notifications since 1981, of which 114 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Culture Media, Selective And Non-differential, Culture Media, Single Biochemical Test, Culture Media, Selective And Differential, Culture Media, Non-selective And Non-differential, Culture Media, Enriched . Use the specialty filter in the sidebar to narrow results.