Enpath Medical Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enpath Medical Incorporated - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Enpath Medical Incorporated has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2004 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Enpath Medical Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enpath Medical Incorporated
2 devices