Eurosets Srl

Eurosets Srl — FDA 510(k) Submissions

Eurosets Srl has submitted 6 FDA 510(k) premarket notifications since 2011, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oxygenator, Cardiopulmonary Bypass . Use the specialty filter in the sidebar to narrow results.