Device Classification Name |
Tourniquet, Nonpneumatic
|
510(k) Number |
K780429 |
Device Name |
TOURNEQUET, NON-PNEUMATIC |
Applicant |
HEMOX, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Correspondent |
HEMOX, INC. |
803 N. Front St. Suite 3 |
McHenry,
IL
60050
|
|
Regulation Number | 878.5900
|
Classification Product Code |
|
Date Received | 03/17/1978 |
Decision Date | 04/18/1978 |
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
|
|
|