Syneron Candela Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Syneron Candela Corporation General & Plastic Surgery ✕
5 devices
Cleared
May 25, 2017
PicoWay Laser System
General & Plastic Surgery
86d
Cleared
Feb 01, 2017
PicoWay Laser System
General & Plastic Surgery
153d
Cleared
Sep 12, 2016
Profound System
General & Plastic Surgery
152d
Cleared
Jul 05, 2016
PicoWay Laser System
General & Plastic Surgery
125d
Cleared
Mar 02, 2016
PicoWay Laser System
General & Plastic Surgery
84d