Oxehealth Limited

Oxehealth Limited — FDA 510(k) Submissions

Oxehealth Limited has submitted 6 FDA 510(k) premarket notifications since 2021, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Software For Optical Camera-based Measurement Of Pulse Rate, Heart Rate, Breathing Rate, And/or Respiratory Rate, Device, Sleep Assessment . Use the specialty filter in the sidebar to narrow results.