Stoeckert Instrumente

Stoeckert Instrumente — FDA 510(k) Submissions

Stoeckert Instrumente has submitted 13 FDA 510(k) premarket notifications since 1982, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Blood, Cardiopulmonary Bypass, Roller Type, Console, Heart-lung Machine, Cardiopulmonary Bypass, Accessory Equipment, Cardiopulmonary Bypass, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, Monitor And/or Control, Level Sensing, Cardiopulmonary Bypass . Use the specialty filter in the sidebar to narrow results.