Device Classification Name |
electrode, ion-specific, chloride
|
510(k) Number |
K060108 |
Device Name |
COBAS INTEGRA CHLORIDE ELCTRODE GEN.2 |
Applicant |
ROCHE DIAGNOSTICS CORP. |
9115 HAGUE RD. |
INDIANAPOLIS,
IN
46250
|
|
Applicant Contact |
CORINA HARPER |
Correspondent |
ROCHE DIAGNOSTICS CORP. |
9115 HAGUE RD. |
INDIANAPOLIS,
IN
46250
|
|
Correspondent Contact |
CORINA HARPER |
Regulation Number | 862.1170
|
Classification Product Code |
|
Date Received | 01/13/2006 |
Decision Date | 02/16/2006 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Summary |
Summary
|
FDA Review |
Decision Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|