Curasan Ag, Frankfurt Facility is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curasan Ag, Frankfurt Facility - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Curasan Ag, Frankfurt Facility has 1 FDA 510(k) cleared medical devices. Based in Garner,, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Curasan Ag, Frankfurt Facility Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Curasan Ag, Frankfurt Facility
1 devices