510(k) K101026 ยท FMI Needle, Hypodermic, Single Lumen
POWERED PD-IO INFUSION SYSTEM, EZ-IO HUMERAL HEAD, POWERED PH-IO
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 27, 2010 |
| Received | Apr 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101026
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.