Scott Laboratories, Inc.

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

Scott Laboratories, Inc. has submitted 16 FDA 510(k) premarket notifications since 1976, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Discs, Strips And Reagents, Microorganism Differentiation, Culture Media, For Isolation Of Pathogenic Neisseria, Stains, Microbiologic, Culture Media, Selective And Non-differential, Culture Media, Non-selective And Differential . Use the specialty filter in the sidebar to narrow results.