Medical Device Manufacturer · US , Lafayette , IN

Ash Access Technology, Inc. - FDA 510(k) Cleared Devices

2 submissions · 0 cleared · Since 2007
2
Total
0
Cleared
0
Denied

Ash Access Technology, Inc. has 0 FDA 510(k) cleared medical devices. Based in Lafayette, US.

Historical record: 0 cleared submissions from 2007 to 2009. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Ash Access Technology, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ash Access Technology, Inc.

2 devices
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