Eurotec, S.R.L.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What Eurotec, S.R.L. makes
Eurotec, S.R.L. manufactures the COMPACT OR COMP-X, a Class II medical device designed for specific diagnostic or therapeutic applications in radiology or imaging procedures.
The COMP-X is regulated under FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Compact Or Comp-X Ref K972365
510(k) 510(k)
Frequently asked questions
How many devices does Eurotec, S.R.L. have in the registry?
The registry currently lists 1 device for Eurotec, S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eurotec, S.R.L.'s devices?
Among its 1 most recently registered device, Eurotec, S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Eurotec, S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eurotec, S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eurotec, S.R.L. in the registry?
The most recently registered devices listed for Eurotec, S.R.L. include COMPACT OR COMP-X.