Genetic Testing Institute

Genetic Testing Institute — FDA 510(k) Submissions

Genetic Testing Institute has submitted 6 FDA 510(k) premarket notifications since 1984, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Platelet Factor 4 Radioimmunoassay, Test, Qualitative And Quantitative Factor Deficiency, Ng1m(a), Antigen, Antiserum, Control . Use the specialty filter in the sidebar to narrow results.