Biotricity

Biotricity — FDA 510(k) Submissions

Biotricity has submitted 3 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrocardiograph, Ambulatory (without Analysis), Recorder, Magnetic Tape, Medical . Use the specialty filter in the sidebar to narrow results.