G.F. S.R.L.
Country not established
- Devices
- 1
What G.F. S.R.L. makes
G.F. S.R.L. manufactures the THD, a medical device designed for [specific clinical use implied by device category—e.g., diagnostic, therapeutic, or monitoring purposes, though exact function is not detailed].
The THD is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Thd Ref K070815
510(k) 510(k)
Frequently asked questions
How many devices does G.F. S.R.L. have in the registry?
The registry currently lists 1 device for G.F. S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list G.F. S.R.L.'s devices?
Among its 1 most recently registered device, G.F. S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do G.F. S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for G.F. S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from G.F. S.R.L. in the registry?
The most recently registered devices listed for G.F. S.R.L. include THD.