FDA 510(k) Applications Submitted by MICOBIOMED CO, LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123007 | 09/27/2012 | VERI-Q MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM, VERI-Q PLUS MGD-1001 BLOOD GLUCOSE MONITORING SYSTEM | MICOBIOMED CO, LTD |
| K123016 | 09/27/2012 | VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS | MICOBIOMED CO, LTD |
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