Device Classification Name |
Control, Hemoglobin
|
510(k) Number |
K993321 |
Device Name |
R&D HGB/GLC WHOLE BLOOD CONTROL |
Applicant |
R & D SYSTEMS, INC. |
614 MCKINLEY PL., N.E. |
MINNEAPOLIS,
MN
55413
|
|
Applicant Contact |
KENNETH T EDDS |
Correspondent |
R & D SYSTEMS, INC. |
614 MCKINLEY PL., N.E. |
MINNEAPOLIS,
MN
55413
|
|
Correspondent Contact |
KENNETH T EDDS |
Regulation Number | 864.8625
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 10/04/1999 |
Decision Date | 11/12/1999 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Hematology
|
510k Review Panel |
Hematology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|