MEDRAD? Imaging Bulk Package Transfer Set
May 2018
133d
Bayer U.S., LLC
1
Total
1
Cleared
0
Denied
Bayer U.S., LLC — FDA 510(k) Submissions
Bayer U.S., LLC has submitted 1 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Iodinated Contrast Media Transfer Tubing Set . Use the specialty filter in the sidebar to narrow results.
1 devices