Medical Device Manufacturer · US , Wayland , MA

Syneron-Candela Corp - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

Syneron-Candela Corp 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 Corp Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Syneron-Candela Corp

1 devices
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