Cybex

Cybex — FDA 510(k) Submissions

Cybex has submitted 9 FDA 510(k) premarket notifications since 1984, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Isokinetic Testing And Evaluation, Goniometer, Ac-powered, Exerciser, Measuring . Use the specialty filter in the sidebar to narrow results.