Device Classification Name |
system, test, blood glucose, over the counter
|
510(k) Number |
K012014 |
Device Name |
MODIFICATION TO BLOOD GLUCOSE MONITORING SYSTEM |
Applicant |
ABBOTT DIABETES CARE INC. |
1360 SOUTH LOOP RD. |
ALAMEDA,
CA
94502 -7000
|
|
Applicant Contact |
EVE A CONNER |
Correspondent |
ABBOTT DIABETES CARE INC. |
1360 SOUTH LOOP RD. |
ALAMEDA,
CA
94502 -7000
|
|
Correspondent Contact |
EVE A CONNER |
Regulation Number | 862.1345
|
Classification Product Code |
|
Subsequent Product Code |
|
Date Received | 06/12/2001 |
Decision Date | 12/05/2001 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|