510(k) K121908 ยท FMI Needle, Hypodermic, Single Lumen
SAFETY INFUSION SET
| Applicant | Greiner Bio-One North America, Inc., Baldwin MD, US |
| Decision | Substantially Equivalent, Jul 25, 2012 |
| Received | Jun 29, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121908
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.