Oxoid , Ltd.

Oxoid , Ltd. — FDA 510(k) Submissions

Oxoid , Ltd. has submitted 36 FDA 510(k) premarket notifications since 1997, of which 36 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Susceptibility Test Discs, Antimicrobial, System, Test, Genotypic Detection, Resistant Markers, Staphylococcus Colonies, Helicobacter Pylori, Kit, Screening, Staphylococcus Aureus, System, Test, Infectious Mononucleosis . Use the specialty filter in the sidebar to narrow results.