Device Classification Name |
System, Test, Blood Glucose, Over The Counter
|
510(k) Number |
K133862 |
Device Name |
ACCU-CHEK AVIVA PLUS SYSTEM |
Applicant |
ROCHE DIAGNOSTICS CORPORATION |
9115 Hague Road |
Indianapolis,
IN
46250
|
|
Applicant Contact |
KHONE SAYSANA |
Correspondent |
ROCHE DIAGNOSTICS CORPORATION |
9115 Hague Road |
Indianapolis,
IN
46250
|
|
Correspondent Contact |
KHONE SAYSANA |
Regulation Number | 862.1345
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 12/19/2013 |
Decision Date | 04/29/2014 |
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
|
Recalls |
CDRH Recalls
|
|
|