Mc3 Incorporated

Mc3 Incorporated — FDA 510(k) Submissions

Mc3 Incorporated has submitted 4 FDA 510(k) premarket notifications since 2017, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dual Lumen Ecmo Cannula, Dilator, Vessel, For Percutaneous Catheterization, Oxygenator, Long Term Support Greater Than 6 Hours . Use the specialty filter in the sidebar to narrow results.