510(k) K032885 ยท FMI Needle, Hypodermic, Single Lumen
VIDAPORT INTRAOSSEOUS INFUSION SYSTEM
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Mar 10, 2004 |
| Received | Sep 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032885
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.