510(k) K051992 ยท FMI Needle, Hypodermic, Single Lumen
POWERED PD-IO INTRAOSSEOUS INFUSION SYSTEM
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Oct 20, 2005 |
| Received | Jul 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051992
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.