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VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123016
510(k) Type
Traditional
Applicant
MICOBIOMED CO, LTD
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/18/2013
Days to Decision
264 days
Submission Type
Summary

VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123016
510(k) Type
Traditional
Applicant
MICOBIOMED CO, LTD
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/18/2013
Days to Decision
264 days
Submission Type
Summary