Novaprobe Incorporated
Country not established
- Devices
- 1
What Novaprobe Incorporated makes
Novaprobe Incorporated manufactures LED light sources designed for medical imaging and diagnostic procedures, providing illumination for enhanced visualization in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Novaprobe Led Light Source Ref K131226
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Novaprobe Incorporated have in the registry?
The registry currently lists 1 device for Novaprobe Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novaprobe Incorporated's devices?
Among its 1 most recently registered device, Novaprobe Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Novaprobe Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Novaprobe Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novaprobe Incorporated in the registry?
The most recently registered devices listed for Novaprobe Incorporated include NOVAPROBE LED LIGHT SOURCE.