Gauss Surgical, Inc.,

Gauss Surgical, Inc., — FDA 510(k) Submissions

Gauss Surgical, Inc., has submitted 6 FDA 510(k) premarket notifications since 2012, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Image Processing Device For Estimation Of External Blood Loss, Counter, Sponge, Surgical . Use the specialty filter in the sidebar to narrow results.