S.A.L.F. Spa

S.A.L.F. Spa — FDA 510(k) Submissions

S.A.L.F. Spa has submitted 6 FDA 510(k) premarket notifications since 2017, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Perfusion, Kidney, Set, Perfusion, Kidney, Disposable, System And Accessories, Isolated Heart, Transport And Preservation . Use the specialty filter in the sidebar to narrow results.