Kbl GmbH - FDA 510(k) Cleared Devices
Recent clearances: KBL 7000 alpha hybridSun, KBL 7900 alpha hybridSun, KBL 8000 alpha hybridSun
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kbl GmbH General & Plastic Surgery ✕
1 devices