Meridian AG - FDA 510(k) Cleared Devices
Recent clearances: MR Q, Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meridian AG Ophthalmic ✕
4 devices