Medical Device Manufacturer · US , Chicago , IL

Wmi Enterprises, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Wmi Enterprises, LLC has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 2 cleared submissions from 2010 to 2010. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Wmi Enterprises, LLC

2 devices
1-2 of 2
Cleared Oct 29, 2010
WMI REPROCESSED DVT WRAP, WMI REPROCESSED THERMAL WRAP MODEL: RD-1000F,...
K101035 · JOW
Cardiovascular · 198d
Cleared Sep 20, 2010
WMI DVT WRAP, WMI THERMAL WRAP MODEL: D-1000F, D-1000C, T-2000A, T-2000B,...
K100969 · JOW
Cardiovascular · 165d
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