Metrovision is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Metrovision - FDA 510(k) Cleared Devices
Recent clearances: Vision Monitor- MonCvONE, Vision Monitor - MonpackONE
2
Total
2
Cleared
0
Denied
Metrovision has 2 FDA 510(k) cleared medical devices. Based in Perenchies, FR.
Last cleared in 2022. Active since 2021. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Metrovision Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Metrovision
2 devices