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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