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FDA 510(k) Applications Submitted by ARTIGLASS SRL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122416
08/08/2012
ARTIGLASS L. O.R. GLASS SYRINGE
ARTIGLASS SRL
K213800
12/06/2021
Artiglass NRFitTM Tip L.O.R. Glass Syringes
Artiglass Srl
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