Medical Device Manufacturer · FR , Vienne

Lokki - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lokki General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Nov 14, 1995

General & Plastic Surgery · 155d