Cox-Uphuff Intl.

Cox-Uphuff Intl. — FDA 510(k) Submissions

Cox-Uphuff Intl. has submitted 11 FDA 510(k) premarket notifications since 1980, of which 11 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tissue Expander And Accessories, Apparatus, Suction, Single Patient Use, Portable, Nonpowered, Apparatus, Suction, Operating-room, Wall Vacuum Powered, Mammary Sizer, Prosthesis, Nose, Internal . Use the specialty filter in the sidebar to narrow results.