Lucid, Inc.
Country not established
- Devices
- 1
What Lucid, Inc. makes
Lucid, Inc. manufactures the Vivascope System (Models 1500 and 3000), a handheld optical imaging device designed for non-invasive skin visualization and diagnostic evaluation.
The Vivascope System is classified as a Class II medical device in the US and is listed under FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Vivascope System, Model 1500, 3000 Ref K080788
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lucid, Inc. have in the registry?
The registry currently lists 1 device for Lucid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lucid, Inc.'s devices?
Among its 1 most recently registered device, Lucid, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lucid, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lucid, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lucid, Inc. in the registry?
The most recently registered devices listed for Lucid, Inc. include VIVASCOPE SYSTEM, MODEL 1500, 3000.