Medical Device Manufacturer · US , Austin , TX

Asuragen, Inc. - FDA 510(k) Cleared Devices

3 submissions · 1 cleared · Since 2012
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.

FDA 510(k) Regulatory Record - Asuragen, Inc.
3 devices
1-3 of 3
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