Livanova Deutschland, GmbH

Livanova Deutschland, GmbH — FDA 510(k) Submissions

Livanova Deutschland, GmbH has submitted 7 FDA 510(k) premarket notifications since 2020, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Console, Heart-lung Machine, Cardiopulmonary Bypass, Controller, Temperature, Cardiopulmonary Bypass, Monitor, Blood-gas, On-line, Cardiopulmonary Bypass, Display, Cathode-ray Tube, Medical . Use the specialty filter in the sidebar to narrow results.