Kuschall of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kuschall of America - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Kuschall of America has 4 FDA 510(k) cleared medical devices. Based in Camarillo, US.
Historical record: 4 cleared submissions from 1995 to 1995. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Kuschall of America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kuschall of America
4 devices