Demasq Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Demasq Limited makes
Demasq Limited manufactures imaging software devices designed for medical diagnostics, focusing on specialized algorithms and processing tools to enhance image analysis in clinical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices, and the products are listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Demasq Imaging Spftware Device Ref K090481
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Demasq Limited have in the registry?
The registry currently lists 1 device for Demasq Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Demasq Limited's devices?
Among its 1 most recently registered device, Demasq Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Demasq Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Demasq Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Demasq Limited in the registry?
The most recently registered devices listed for Demasq Limited include DEMASQ IMAGING SPFTWARE DEVICE.