Dutchland Laboratories, Inc.

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

Dutchland Laboratories, Inc. has submitted 75 FDA 510(k) premarket notifications since 1981, of which 75 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media And Components, Synthetic Cell And Tissue Culture, Sera, Animal And Human, Staphylococcus Aureus Somatic Antigens, Formulations, Balanced Salt Solutions, Reagent, Complement . Use the specialty filter in the sidebar to narrow results.