Bayer U.S., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bayer U.S., LLC - FDA 510(k) Cleared Devices
Recent clearances: MEDRAD® Imaging Bulk Package Transfer Set
1
Total
1
Cleared
0
Denied
Bayer U.S., LLC has 1 FDA 510(k) cleared medical devices. Based in Indianola, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bayer U.S., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bayer U.S., LLC
1 devices