510(k) K160532 ยท FMI Needle, Hypodermic, Single Lumen
Greiner Holdex
| Applicant | Greiner Bio-One Na, Inc., Monroe NC, US |
| Decision | Substantially Equivalent, Nov 3, 2016 |
| Received | Feb 26, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160532
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.