Alliance Instruments
Country not established
- Devices
- 1
What Alliance Instruments makes
Alliance Instruments manufactures the INTEGRITI PATIENT MONITOR, a medical device used for patient monitoring.
The company is based in the US, and its device is classified as Class II and listed in the FDA 510(k) registry.
Catalogue
Integriti Patient Monitor Ref K980688
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alliance Instruments have in the registry?
The registry currently lists 1 device for Alliance Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alliance Instruments's devices?
Among its 1 most recently registered device, Alliance Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Alliance Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alliance Instruments's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alliance Instruments in the registry?
The most recently registered devices listed for Alliance Instruments include INTEGRITI PATIENT MONITOR.