Ralco S.R.L.

Ralco S.R.L. — FDA 510(k) Submissions

Ralco S.R.L. has submitted 6 FDA 510(k) premarket notifications since 1995, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Collimator, Automatic, Radiographic, Device, Beam Limiting, X-ray, Diagnostic, Collimator, Manual, Radiographic . Use the specialty filter in the sidebar to narrow results.