Device Classification Name |
test, qualitative and quantitative factor deficiency
|
510(k) Number |
K981200 |
Device Name |
IL TEST PLASMINOGEN |
Applicant |
INSTRUMENTATION LABORATORY CO. |
113 HARTWELL AVE. |
LEXINGTON,
MA
02173
|
|
Applicant Contact |
CAROL MARBLE |
Correspondent |
INSTRUMENTATION LABORATORY CO. |
113 HARTWELL AVE. |
LEXINGTON,
MA
02173
|
|
Correspondent Contact |
CAROL MARBLE |
Regulation Number | 864.7290
|
Classification Product Code |
|
Date Received | 04/02/1998 |
Decision Date | 05/26/1998 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Hematology
|
510k Review Panel |
Hematology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|