Id Biomedical Corp.

Id Biomedical Corp. — FDA 510(k) Submissions

Id Biomedical Corp. has submitted 3 FDA 510(k) premarket notifications since 1999, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Genotypic Detection, Resistant Markers, Staphylococcus Colonies, System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species . Use the specialty filter in the sidebar to narrow results.