C.S.O. S.R.L.
Country not established FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What C.S.O. S.R.L. makes
C.S.O. S.R.L. manufactures ophthalmic diagnostic devices, including the F 900 retinal imaging system and the COBRA fundus camera for retinal photography, as well as the MS-39 slit-lamp biomicroscope for anterior segment examination.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
F 900 Ref K022054
510(k) 510(k)Cobra Fundus Camera Ref K132987
510(k) 510(k)Ms-39 Ref K221601
510(k) 510(k)
FDA establishments
- C.S.O. S.R.L. Scandicci Firenze · IT Other ID 4196
Frequently asked questions
How many devices does C.S.O. S.R.L. have in the registry?
The registry currently lists 3 devices for C.S.O. S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.S.O. S.R.L.'s devices?
Among its 3 most recently registered devices, C.S.O. S.R.L. has devices listed in FDA 510(k) (3 devices).
What risk classes do C.S.O. S.R.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for C.S.O. S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C.S.O. S.R.L. in the registry?
The most recently registered devices listed for C.S.O. S.R.L. include F 900, COBRA FUNDUS CAMERA and MS-39.
Which FDA establishments are linked to C.S.O. S.R.L.?
1 FDA establishment is linked to C.S.O. S.R.L. in the registry; they are listed on the company page.