Difco Laboratories, Inc.

Difco Laboratories, Inc. — FDA 510(k) Submissions

Difco Laboratories, Inc. has submitted 121 FDA 510(k) premarket notifications since 1979, of which 121 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Susceptibility Test Discs, Antimicrobial, Discs, Strips And Reagents, Microorganism Differentiation, Antisera, All Groups, Streptococcus Spp., Cells, Animal And Human, Cultured, Culture Media, Single Biochemical Test . Use the specialty filter in the sidebar to narrow results.