Simavita Pty Limited

Simavita Pty Limited — FDA 510(k) Submissions

Simavita Pty Limited has submitted 1 FDA 510(k) premarket notifications since 2013, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Alarm, Conditioned Response Enuresis . Use the specialty filter in the sidebar to narrow results.