Empatica S.R.L.

Empatica S.R.L. — FDA 510(k) Submissions

Empatica S.R.L. has submitted 8 FDA 510(k) premarket notifications since 2018, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Physiological Signal Based Seizure Monitoring System, Monitor, Physiological, Patient (without Arrhythmia Detection Or Alarms), Device, Sleep Assessment, Oximeter . Use the specialty filter in the sidebar to narrow results.