510(k) K142518 ยท FMF Syringe, Piston
HumaPen Luxura
| Applicant | Eli Lilly and Company, Indianapolis IN, US |
| Decision | Substantially Equivalent, Jun 5, 2015 |
| Received | Sep 8, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142518
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.