Medical Device Manufacturer · US , Indianapolis , IN

Eli Lilly and Company - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006
Official Website
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Eli Lilly and Company General Hospital ✕
5 devices
1-5 of 5
Cleared Sep 16, 2022
Tempo Smart Button
K212217 · QOG
General Hospital · 427d
Cleared Dec 22, 2016
Go Dose System
K160949 · NDC
General Hospital · 261d
Cleared Jun 05, 2015
HumaPen Luxura
K142518 · FMF
General Hospital · 270d
Cleared Aug 17, 2010
HUMAPEN LUXURA HD
K100988 · FMF
General Hospital · 130d
Cleared Apr 07, 2006
HUMAPEN MEMOIR
K053563 · FMF
General Hospital · 107d
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