Medical Device Manufacturer · US , Indianapolis , IN

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

2 submissions · 2 cleared · Since 2015

Recent clearances: HumaPen Savvio, HumanPen Ergo II

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Eli Lilly and Company, Inc. General Hospital ✕

2 devices

1-2 of 2

Cleared Jun 03, 2016

General Hospital · 86d

Cleared Dec 30, 2015

HumanPen Ergo II

General Hospital · 190d