Syneron-Candela - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Syneron-Candela has 1 FDA 510(k) cleared medical devices. Based in Wayland, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Syneron-Candela Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syneron-Candela
1 devices