Spectrum Medical S.R.L.

Spectrum Medical S.R.L. — FDA 510(k) Submissions

Spectrum Medical S.R.L. has submitted 6 FDA 510(k) premarket notifications since 2024, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Blood, Cardiopulmonary Bypass, Non-roller Type, Oxygenator, Cardiopulmonary Bypass, Reservoir, Blood, Cardiopulmonary Bypass, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, Heat-exchanger, Cardiopulmonary Bypass . Use the specialty filter in the sidebar to narrow results.