Candela Corp. - FDA 510(k) Cleared Devices
Recent clearances: Vbeam Prima Laser System, CANDELA GENTLELASE FAMILY OF LASER SYSTEMS, CANDELA GENTLEMAX FAMILY OF LASER SYSTEM
48
Total
48
Cleared
0
Denied
FDA 510(k) Regulatory Record - Candela Corp. Gastroenterology & Urology ✕
1 devices