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CLOVER A1C/GLYCOSYLATED HEMOGLOBIN MONITOR & BLOOD GLUCOSE MONITOR, MODEL IGM-0023

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082275
510(k) Type
Traditional
Applicant
Infopia Co, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2010
Days to Decision
521 days
Submission Type
Summary

CLOVER A1C/GLYCOSYLATED HEMOGLOBIN MONITOR & BLOOD GLUCOSE MONITOR, MODEL IGM-0023

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082275
510(k) Type
Traditional
Applicant
Infopia Co, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/14/2010
Days to Decision
521 days
Submission Type
Summary