Tenet Medical Engineering

Tenet Medical Engineering — FDA 510(k) Submissions

Tenet Medical Engineering has submitted 3 FDA 510(k) premarket notifications since 1996, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Obstetrical, Manual (and Accessories), Table, Operating-room, Ac-powered, Chair, Surgical, Ac-powered . Use the specialty filter in the sidebar to narrow results.