Medical Device Manufacturer · GB , Basildon

Vitage Led, Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017

Recent clearances: LIGHTFUSION LED SYSTEM

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FDA 510(k) Regulatory Record - Vitage Led, Ltd. General & Plastic Surgery ✕

1 devices
1-1 of 1
Cleared Mar 24, 2017
LIGHTFUSION LED SYSTEM
K162556 · GEX
General & Plastic Surgery · 191d
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