Micro Media Laboratories

Micro Media Laboratories — FDA 510(k) Submissions

Micro Media Laboratories has submitted 52 FDA 510(k) premarket notifications since 1979, of which 52 received clearance as substantially equivalent to a predicate device.

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