510(k) K151686 ยท FMF Syringe, Piston
HumanPen Ergo II
| Applicant | Eli Lilly and Company, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Dec 30, 2015 |
| Received | Jun 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151686
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.