|
|
| Document Number | K192859 |
| Test Name | i-SENS, Inc., CareSens S Clear BT Blood Glucose Monitoring System |
| Manufacturer Name | i-SENS, Inc. |
| Consumer Information Phone Number | (800)429-5001 |
| Test Type | Glucose monitoring devices (FDA cleared/home use) |
| Effective Date | 01/27/2020 |
| |
| Device Classification Name |
System, Test, Blood Glucose, Over The Counter
|
| 510(k) Number |
K192859 |
| Device Name |
CareSens S Clear BT Blood Glucose Monitoring System |
| Applicant |
| i-SENS, Inc. |
| 43, Banpo-daero 28-gil, Seocho-gu |
|
Seoul,
KR
06646
|
|
| Applicant Contact |
Joon Ho Jung |
| Correspondent |
| i-SENS, Inc. |
| 43, Banpo-daero 28-gil, Seocho-gu |
|
Seoul,
KR
06646
|
|
| Correspondent Contact |
Joon Ho Jung |
| Regulation Number | 862.1345 |
| Classification Product Code |
|
| Date Received | 10/04/2019 |
| Decision Date | 01/24/2020 |
| Decision |
Substantially Equivalent
(SESE) |
| Regulation Medical Specialty |
Clinical Chemistry
|
| 510k Review Panel |
Clinical Chemistry
|
| Statement |
Statement
|
| FDA Review |
Decision Summary
|
| Type |
Special
|
| Reviewed by Third Party |
No
|
| Combination Product |
No
|
Predetermined Change Control Plan Authorized |
No
|
|
|
|