Oasis Medical, Inc.

Oasis Medical, Inc. — FDA 510(k) Submissions

Oasis Medical, Inc. has submitted 17 FDA 510(k) premarket notifications since 1991, of which 17 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plug, Punctum, Keratome, Ac-powered, Unit, Phacofragmentation, Collagen Corneal Shield, Tonometer, Manual . Use the specialty filter in the sidebar to narrow results.