Plancon Instruments - FDA 510(k) Cleared Devices
Recent clearances: PLANCON MICROLAMELLAR KERATOME EVOLUTION, PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES)
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Plancon Instruments Ophthalmic ✕
3 devices