Microvision, Inc.

Microvision, Inc. — FDA 510(k) Submissions

Microvision, Inc. has submitted 3 FDA 510(k) premarket notifications since 1998, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plug, Scleral, Implant, Orbital, Extra-ocular, Image, Illumination, Fiberoptic, For Endoscope . Use the specialty filter in the sidebar to narrow results.