Device Classification Name |
System, Test, C-Reactive Protein
|
510(k) Number |
K032336 |
Device Name |
TINA-QUANT CRP (LATEX) |
Applicant |
ROCHE DIAGNOSTICS CORP. |
9115 HAGUE RD. |
INDIANAPOLIS,
IN
46250
|
|
Applicant Contact |
SHERRI L COENEN |
Correspondent |
ROCHE DIAGNOSTICS CORP. |
9115 HAGUE RD. |
INDIANAPOLIS,
IN
46250
|
|
Correspondent Contact |
SHERRI L COENEN |
Regulation Number | 866.5270
|
Classification Product Code |
|
Date Received | 07/29/2003 |
Decision Date | 08/05/2003 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Immunology
|
510k Review Panel |
Clinical Chemistry
|
Summary |
Summary
|
FDA Review |
Decision Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|