Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Eli Lilly and Company

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K212217 Tempo Smart ButtonQOG2022-09-16 View
510(k) K160949 Go Dose SystemNDC2016-12-22 View
510(k) K100988 HUMAPEN LUXURA HDFMF2010-08-17 View
510(k) K053563 HUMAPEN MEMOIRFMF2006-04-07 View
↑