C.S.O. S.R.L. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
C.S.O. S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: MS-39
3
Total
3
Cleared
0
Denied
C.S.O. S.R.L. has 3 FDA 510(k) cleared medical devices. Based in Williamsville, US.
Last cleared in 2023. Active since 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by C.S.O. S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.
FDA 510(k) Regulatory Record - C.S.O. S.R.L.
3 devices