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Artiglass Srl
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K213800
Artiglass NRFitTM Tip L.O.R. Glass Syringes
May 19, 2022
K122416
ARTIGLASS L. O.R. GLASS SYRINGE
May 3, 2013