Aesculap-Meditec North America - FDA 510(k) Cleared Devices
Recent clearances: LASER SYSTEM RUBYSTAR WITH Q-SWITCH AND NORMAL MODE, MEDITEC LINK, DERMABLATE ER: YAG LASER SYSTEM
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aesculap-Meditec North America Ophthalmic ✕
2 devices