Kerr Hearing Aid Laboratory is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kerr Hearing Aid Laboratory - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kerr Hearing Aid Laboratory has 1 FDA 510(k) cleared medical devices. Based in Titusville, US.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Kerr Hearing Aid Laboratory Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kerr Hearing Aid Laboratory
1 devices