510(k) K100988 ยท FMF Syringe, Piston
HUMAPEN LUXURA HD
| Applicant | Eli Lilly and Company, Indianapolis IN, US |
| Decision | Substantially Equivalent, Aug 17, 2010 |
| Received | Apr 9, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100988
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.