Ab Medica Sas

Ab Medica Sas — FDA 510(k) Submissions

Ab Medica Sas has submitted 3 FDA 510(k) premarket notifications since 2014, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.