K & S Medicorp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
K & S Medicorp - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
K & S Medicorp has 3 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 3 cleared submissions from 1986 to 1986. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by K & S Medicorp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K & S Medicorp
3 devices