510(k) K080235 ยท FMI Needle, Hypodermic, Single Lumen
SAFETY INFUSION SET
| Applicant | Greiner Bio-One Vacuette North America, Hydes MD, US |
| Decision | Substantially Equivalent, Apr 24, 2008 |
| Received | Jan 30, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080235
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.