Sentec AG

Sentec AG — FDA 510(k) Submissions

Sentec AG has submitted 5 FDA 510(k) premarket notifications since 2007, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Carbon-dioxide, Cutaneous, Oximeter, Ventilatory Electrical Impedance Tomograph . Use the specialty filter in the sidebar to narrow results.