Enraf-Nonius, B.V.

Enraf-Nonius, B.V. — FDA 510(k) Submissions

Enraf-Nonius, B.V. has submitted 5 FDA 510(k) premarket notifications since 2003, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Equipment, Traction, Powered, Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat, Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat, Stimulator, Muscle, Powered, Electrode, Cutaneous . Use the specialty filter in the sidebar to narrow results.