FDA 510(k) Applications Submitted by Eli Lilly and Company, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K151686 | 06/23/2015 | HumanPen Ergo II | ELI LILLY AND COMPANY, INC. |
| K160668 | 03/09/2016 | HumaPen Savvio | Eli Lilly and Company, Inc. |
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