Ssgi Prowess Systems
Country not established
- Devices
- 2
What Ssgi Prowess Systems makes
Ssgi Prowess Systems manufactures the PROWESS PRO-SIM, a medical simulation device designed for training purposes, along with modifications to enhance its functionality.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Prowess Pro-Sim Ref K980379
Regimes: 510(k) Registry: 510(k)Modification To Prowess Pro-Sim Ref K984196
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ssgi Prowess Systems have in the registry?
The registry currently lists 2 devices for Ssgi Prowess Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ssgi Prowess Systems's devices?
Among its 2 most recently registered devices, Ssgi Prowess Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Ssgi Prowess Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ssgi Prowess Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ssgi Prowess Systems in the registry?
The most recently registered devices listed for Ssgi Prowess Systems include PROWESS PRO-SIM and MODIFICATION TO PROWESS PRO-SIM.