510(k) K213800 · QEH Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact
Artiglass NRFitTM Tip L.O.R. Glass Syringes
| Applicant | Artiglass Srl, Due Carrare, IT |
| Decision | Substantially Equivalent, May 19, 2022 |
| Received | Dec 6, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K213800
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.