Device Classification Name |
glucose oxidase, glucose
|
510(k) Number |
K113636 |
Device Name |
BLOOD GLUCOSE MONITORING SYSTEM (GLUCOSE OXIDASE) |
Applicant |
PHILOSYS CO. LTD. |
304 PARK AVENUE SOUTH |
SUITE 218 |
NEW YORK,
NY
10010
|
|
Applicant Contact |
LINDA CHAN |
Correspondent |
PHILOSYS CO. LTD |
304 PARK AVENUE SOUTH |
SUITE 218 |
NEW YORK,
NY
10010
|
|
Correspondent Contact |
LINDA CHAN |
Regulation Number | 862.1345
|
Classification Product Code |
|
Subsequent Product Codes |
|
Date Received | 12/09/2011 |
Decision Date | 03/08/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Clinical Chemistry
|
510k Review Panel |
Clinical Chemistry
|
Summary |
Summary
|
FDA Review |
Decision Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|