Iris Diagnostics

Iris Diagnostics — FDA 510(k) Submissions

Iris Diagnostics has submitted 2 FDA 510(k) premarket notifications since 2007, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Urinalysis Controls (assayed And Unassayed), Counter, Cell, Automated (particle Counter) . Use the specialty filter in the sidebar to narrow results.