Argus Photonics Group - FDA 510(k) Cleared Devices
Recent clearances: ACCU-PULSE 1000 CO2 SURGICAL LASER SYSTEM, ACCU-PULSE CARBON DIOXIDE LASER SYSTEM
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Argus Photonics Group General & Plastic Surgery ✕
2 devices