Medical Device Manufacturer · FR , Prunay Le Gillon

Luneau Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2015
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Luneau Sas Ophthalmic ✕

2 devices
1-2 of 2
Cleared Apr 24, 2017
VX130 Ophthalmic Diagnostic Device
K162067 · HKX
Ophthalmic · 272d
Cleared Jun 01, 2015
VX120 Ophthalmic Diagnostic Device
K143086 · HKX
Ophthalmic · 217d
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