510(k) K052195 ยท FMI Needle, Hypodermic, Single Lumen
EZ-MIO MANUAL DRIVER
| Applicant | Vidacare Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Nov 2, 2005 |
| Received | Aug 11, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052195
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.