Device Classification Name |
Tourniquet, Nonpneumatic
|
510(k) Number |
K872003 |
Device Name |
KINDERWRAP |
Applicant |
THE KINDER CO. |
411 GREENLAWN |
YPSILANTI,
MI
48198
|
|
Applicant Contact |
TIM KINDER |
Correspondent |
THE KINDER CO. |
411 GREENLAWN |
YPSILANTI,
MI
48198
|
|
Correspondent Contact |
TIM KINDER |
Regulation Number | 878.5900
|
Classification Product Code |
|
Date Received | 05/26/1987 |
Decision Date | 06/23/1987 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
General & Plastic Surgery
|
510k Review Panel |
General & Plastic Surgery
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|