Italian Engineering S.r.l.
ItalyFDA applicant, unverified
- Devices
- 1
What Italian Engineering S.r.l. makes
Italian Engineering S.R.L. manufactures the ATTIVA, a medical device designed for [specific application not detailed in data]. The product is intended for [clinical use or purpose not specified in data].
The ATTIVA 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
Attiva Ref K220505
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Italian Engineering S.R.L. have in the registry?
The registry currently lists 1 device for Italian Engineering S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Italian Engineering S.R.L.'s devices?
Among its 1 most recently registered device, Italian Engineering S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Italian Engineering S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Italian Engineering S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Italian Engineering S.R.L. in the registry?
The most recently registered devices listed for Italian Engineering S.R.L. include ATTIVA.