510(k) K160668 ยท FMF Syringe, Piston
HumaPen Savvio
| Applicant | Eli Lilly and Company, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jun 3, 2016 |
| Received | Mar 9, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160668
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.