FDA 510(k) Applications Submitted by OK BIOTECH CO., LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K132633 |
08/22/2013 |
OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM |
OK BIOTECH CO., LTD. |
| K142785 |
09/26/2014 |
PRODIGY iConnect Blood Glucose Monitoring System |
OK BIOTECH CO., LTD. |
| K160038 |
01/07/2016 |
UniStrip1 Generic Blood Glucose Test Strips |
OK BIOTECH CO., LTD. |
| K090609 |
03/06/2009 |
OKMETER MATCH BLOOD GLUCOSE MONITORING SYSTEM |
OK BIOTECH CO., LTD. |
| K141914 |
07/15/2014 |
PRODIGY AUTOCODE EJECT BLOOD GLUCOSE MONITORING SYSTEM |
OK BIOTECH CO., LTD. |
| K162430 |
08/31/2016 |
UniStrip1 Generic Blood Glucose Test Strips |
OK BIOTECH CO., LTD. |
| K152599 |
09/11/2015 |
PRODIGY ASTRO Blood Glucose Monitoring System, PRODIGY ASTRO PRO Blood Glucose Monitoring System |
OK BIOTECH CO., LTD. |
| K063026 |
10/02/2006 |
OK METER BLOOD GLUCOSE MONITORING SYSTEM |
OK BIOTECH CO., LTD. |
| K213061 |
09/22/2021 |
SuperCheck Pro Blood Glucose Monitoring System |
OK BioTech Co., Ltd. |
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