Diagnon Corp.

Diagnon Corp. — FDA 510(k) Submissions

Diagnon Corp. has submitted 6 FDA 510(k) premarket notifications since 1983, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Radioassay, Vitamin B12, Acid, Folic, Radioimmunoassay, Device, Specimen Collection, Antisera, Fluorescent, Herpesvirus Hominis 1,2, Culture Media, Propagating Transport . Use the specialty filter in the sidebar to narrow results.