Cortronic Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cortronic Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cortronic Corp. has 2 FDA 510(k) cleared medical devices. Based in Northport, US.
Historical record: 2 cleared submissions from 1986 to 1989. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cortronic Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cortronic Corp.
2 devices