510(k) K243486 ยท LHI Set, I.V. Fluid Transfer
SmartSiteTM Vented Vial Access Device
| Applicant | Yukon Medical, LLC, Durham NC, US |
| Decision | Substantially Equivalent, Dec 6, 2024 |
| Received | Nov 8, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243486
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.