Mettler Electronics Corp.

Mettler Electronics Corp. — FDA 510(k) Submissions

Mettler Electronics Corp. has submitted 32 FDA 510(k) premarket notifications since 1985, of which 28 received clearance as substantially equivalent to a predicate device.

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