510(k) K132583 ยท FMI Needle, Hypodermic, Single Lumen
EZ-IO INTRAOSSEOUS INFUSION SYSTEM
| Applicant | Vidacare Corporation, Shavano Park TX, US |
| Decision | Substantially Equivalent, Feb 11, 2014 |
| Received | Aug 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132583
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.