Deroyal

Deroyal — FDA 510(k) Submissions

Deroyal has submitted 5 FDA 510(k) premarket notifications since 2002, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gown, Surgical, Drape, Surgical, Catheter, Upper Urinary Tract, Container, Empty, For Collection & Processing Of Blood & Blood Components . Use the specialty filter in the sidebar to narrow results.