Medical Device Manufacturer · IT , Dueville (Vi)

Biotec Italia, Srl - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Recent clearances: XLase Plus

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Biotec Italia, Srl General & Plastic Surgery

1 devices
1-1 of 1
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