Visual Pathways, Inc.
Country not established
- Devices
- 1
What Visual Pathways, Inc. makes
Visual Pathways, Inc. manufactures a fundus autoimager, a device designed for automated imaging of the retina to capture detailed photographs of the back of the eye, including the optic disc, macula, and retinal blood vessels.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The fundus autoimager is listed in the FDA’s 510(k) database.
Catalogue
Fundus Autoimager Ref K020888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visual Pathways, Inc. have in the registry?
The registry currently lists 1 device for Visual Pathways, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visual Pathways, Inc.'s devices?
Among its 1 most recently registered device, Visual Pathways, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Visual Pathways, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Visual Pathways, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visual Pathways, Inc. in the registry?
The most recently registered devices listed for Visual Pathways, Inc. include FUNDUS AUTOIMAGER.