Bioserenity Sas

Bioserenity Sas — FDA 510(k) Submissions

Bioserenity Sas has submitted 3 FDA 510(k) premarket notifications since 2018, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Full-montage Standard Electroencephalograph, Transmitters And Receivers, Electrocardiograph, Telephone . Use the specialty filter in the sidebar to narrow results.