Medical Diagnostics, Ca.

Medical Diagnostics, Ca. — FDA 510(k) Submissions

Medical Diagnostics, Ca. has submitted 4 FDA 510(k) premarket notifications since 1983, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control, System, Test, Thyroid Autoantibody, Endoscope, Fiber Optic, Thin Layer Chromatography, Morphine . Use the specialty filter in the sidebar to narrow results.