Device Classification Name |
tourniquet, nonpneumatic
|
510(k) Number |
K881398 |
Device Name |
TOURNIQUET |
Applicant |
BARRETTA PRODUCTS, RESEARCH AND DEVELOPMENT, INC. |
130 DURHU DRIVE, DEPT. D |
MOBILE,
AL
36608
|
|
Applicant Contact |
CARL BARRETT |
Correspondent |
BARRETTA PRODUCTS, RESEARCH AND DEVELOPMENT, INC. |
130 DURHU DRIVE, DEPT. D |
MOBILE,
AL
36608
|
|
Correspondent Contact |
CARL BARRETT |
Regulation Number | 878.5900
|
Classification Product Code |
|
Date Received | 04/04/1988 |
Decision Date | 04/29/1988 |
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
|
|
|