Thd Spa

Thd Spa — FDA 510(k) Submissions

Thd Spa has submitted 13 FDA 510(k) premarket notifications since 2008, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Anoscope And Accessories, Monitor, Ultrasonic, Nonfetal, Monitor, Esophageal Motility, Anorectal Motility, And Tube, System, Imaging, Pulsed Echo, Ultrasonic, Ligator, Hemorrhoidal . Use the specialty filter in the sidebar to narrow results.