Viggo-Spectramed
Country not established
- Devices
- 1
What Viggo-Spectramed makes
Viggo-Spectramed manufactures core monitoring systems, including models SP1475, 6275, 5607, 5708, and 4575, designed for patient vital sign tracking in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viggo-Spectramed have in the registry?
The registry currently lists 1 device for Viggo-Spectramed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viggo-Spectramed's devices?
Among its 1 most recently registered device, Viggo-Spectramed has devices listed in FDA 510(k) (1 device).
What risk classes do Viggo-Spectramed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Viggo-Spectramed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Viggo-Spectramed in the registry?
The most recently registered devices listed for Viggo-Spectramed include CORE MONITORING SYSTEM-SP1475/6275/5607/5708/4575.