Ge Healthcare Filand OY

Ge Healthcare Filand OY — FDA 510(k) Submissions

Ge Healthcare Filand OY has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Index-generating Electroencephalograph Software . Use the specialty filter in the sidebar to narrow results.