Euro-Diagnostica AB

Euro-Diagnostica AB — FDA 510(k) Submissions

Euro-Diagnostica AB has submitted 6 FDA 510(k) premarket notifications since 1997, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antibodies, Anti-cyclic Citrullinated Peptide (ccp), Test System, Antineutrophil Cytoplasmic Antibodies (anca), Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control . Use the specialty filter in the sidebar to narrow results.