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 — 2 products

Total Devices2
Categories2
Latest FDA decision2022-09-16
TypeNumberDevice NameCodeDateActions
510(k) K212217 Tempo Smart ButtonQOG2022-09-16 View
510(k) K160949 Go Dose SystemNDC2016-12-22 View