Simavita Pty Limited
Country not established
- Devices
- 1
What Simavita Pty Limited makes
Simavita Pty Limited manufactures the SIM, a medical device designed for [specific function or application not detailed in provided data]. The product is intended for [clinical context or use case not specified in data].
The SIM falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sim Ref K130951
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Simavita Pty Limited have in the registry?
The registry currently lists 1 device for Simavita Pty Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Simavita Pty Limited's devices?
Among its 1 most recently registered device, Simavita Pty Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Simavita Pty Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Simavita Pty Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Simavita Pty Limited in the registry?
The most recently registered devices listed for Simavita Pty Limited include SIM.