Cuda Products Co.

Cuda Products Co. — FDA 510(k) Submissions

Cuda Products Co. has submitted 17 FDA 510(k) premarket notifications since 1988, of which 17 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Light, Surgical, Floor Standing, Light, Surgical, Fiberoptic, Laparoscope, Gynecologic (and Accessories), Powered Laser Surgical Instrument, Light Source, Fiberoptic, Routine . Use the specialty filter in the sidebar to narrow results.