Kay Elemetrics Corp.

Kay Elemetrics Corp. — FDA 510(k) Submissions

Kay Elemetrics Corp. has submitted 5 FDA 510(k) premarket notifications since 1992, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laryngostroboscope, Monitor, Esophageal Motility, Anorectal Motility, And Tube, Electroglottograph, System, Image Processing, Radiological . Use the specialty filter in the sidebar to narrow results.