FDA 510(k) Applications Submitted by MIKE WILFORD

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100969	04/08/2010	WMI DVT WRAP, WMI THERMAL WRAP MODEL: D-1000F, D-1000C, T-2000A, T-2000B, T-2000KF, T-2000S, T-2000N	WMI ENTERPRISES LLC
K101035	04/14/2010	WMI REPROCESSED DVT WRAP, WMI REPROCESSED THERMAL WRAP MODEL: RD-1000F, RD-1000C, RT 2000A, RT 2000B, RT 2000KF, RT 2000	WMI ENTERPRISES LLC