Medical Device Manufacturer · US , Indianapolis , IN

Promex Technologies, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011
1
Total
1
Cleared
0
Denied

Promex Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Promex Technologies, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Promex Technologies, LLC

1 devices
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