Device Classification Name |
Sleeve, Limb, Compressible
|
510(k) Number |
K100969 |
Device Name |
WMI DVT WRAP, WMI THERMAL WRAP MODEL: D-1000F, D-1000C, T-2000A, T-2000B, T-2000KF, T-2000S, T-2000N |
Applicant |
WMI ENTERPRISES LLC |
1017 W. WASHINGTON, 2J |
CHICAGO,
IL
60607
|
|
Applicant Contact |
MIKE WILFORD |
Correspondent |
WMI ENTERPRISES LLC |
1017 W. WASHINGTON, 2J |
CHICAGO,
IL
60607
|
|
Correspondent Contact |
MIKE WILFORD |
Regulation Number | 870.5800
|
Classification Product Code |
|
Date Received | 04/08/2010 |
Decision Date | 09/20/2010 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|