Rms Div.

Rms Div. — FDA 510(k) Submissions

Rms Div. has submitted 10 FDA 510(k) premarket notifications since 1989, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Radiographic, Tilting, Device, Spot-film, Alloy, Other Noble Metal, Alloy, Gold-based Noble Metal, Probe, Periodontic . Use the specialty filter in the sidebar to narrow results.