Prestige Ameritech

Prestige Ameritech — FDA 510(k) Submissions

Prestige Ameritech has submitted 5 FDA 510(k) premarket notifications since 2006, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Mask, Surgical, Respirator, Surgical, Pediatric/child Facemask, Surgical Mask With Antimicrobial/antiviral Agent . Use the specialty filter in the sidebar to narrow results.