Medical Device Manufacturer · IT , Due Carrare Padova

Artiglass Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Artiglass Srl General Hospital ✕

1 devices

1-1 of 1

Cleared May 03, 2013

ARTIGLASS L. O.R. GLASS SYRINGE

General Hospital · 268d