Asuragen, Inc. - FDA 510(k) Cleared Devices
3
Total
1
Cleared
2
Denied
Asuragen, Inc. has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Medical Genetics.
Browse the FDA 510(k) cleared devices submitted by Asuragen, Inc. Filter by specialty or product code using the sidebar.
3 devices