Device Classification Name |
control, cell counter, normal and abnormal
|
510(k) Number |
K891907 |
Device Name |
QBC(R) CENTRIFUGAL HEMATOLOGY CONTR/MULTI MODIFIED |
Applicant |
R & D SYSTEMS, INC. |
614 MCKINLEY PL., N.E. |
MINNEAPOLIS,
MN
55413
|
|
Applicant Contact |
KAREN VISKOCHIL |
Correspondent |
R & D SYSTEMS, INC. |
614 MCKINLEY PL., N.E. |
MINNEAPOLIS,
MN
55413
|
|
Correspondent Contact |
KAREN VISKOCHIL |
Regulation Number | 864.8625
|
Classification Product Code |
|
Date Received | 03/27/1989 |
Decision Date | 04/11/1989 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Hematology
|
510k Review Panel |
Hematology
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|