510(k) K232943 · QNQ Low Dead Space Piston Syringe
Hypodermic Needle-Pro® EDGE Safety Device with Low Dead Space Syringe
| Applicant | Smiths Medical Asd, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, May 31, 2024 |
| Received | Sep 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232943
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.