Device Classification Name |
sleeve, limb, compressible
|
510(k) Number |
K841235 |
Device Name |
MEDO MEDOMER MBF-100 II |
Applicant |
MEDO U.S.A., INC. |
P.O. BOX 129 |
WOOD DALE,
IL
60191
|
|
Applicant Contact |
HIROSHI OKAZAKI |
Correspondent |
MEDO U.S.A., INC. |
P.O. BOX 129 |
WOOD DALE,
IL
60191
|
|
Correspondent Contact |
HIROSHI OKAZAKI |
Regulation Number | 870.5800
|
Classification Product Code |
|
Date Received | 03/22/1984 |
Decision Date | 11/19/1984 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|