Device Classification Name |
Tourniquet, Pneumatic
|
510(k) Number |
K813231 |
Device Name |
TOURNIQUET |
Applicant |
ASPEN LABORATORIES, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
ASPEN LABORATORIES, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.5910
|
Classification Product Code |
|
Date Received | 11/17/1981 |
Decision Date | 12/14/1981 |
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
|
|
|