Vioptix, Inc.

Vioptix, Inc. — FDA 510(k) Submissions

Vioptix, Inc. has submitted 9 FDA 510(k) premarket notifications since 2005, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oximeter, Tissue Saturation, Device, Anastomotic, Microvascular . Use the specialty filter in the sidebar to narrow results.