Eli Lilly and Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eli Lilly and Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Eli Lilly and Co. has 2 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 2 cleared submissions from 1998 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Eli Lilly and Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eli Lilly and Co.
2 devices