510(k) K202492 ยท FMI Needle, Hypodermic, Single Lumen
EZ-IO Intraosseous Vascular Access System
| Applicant | Teleflex Medical, Morrisville NC, US |
| Decision | Substantially Equivalent, Mar 22, 2021 |
| Received | Aug 31, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202492
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.