510(k) K982842 ยท FMF Syringe, Piston
HUMAPEN AND HUMAPEN ERGO
| Applicant | Eli Lilly and Co., Indianapolis IN, US |
| Decision | Substantially Equivalent, Sep 25, 1998 |
| Received | Aug 12, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982842
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.