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QUICKTEK BLOOD GLUCOSE SYSTEM, QUICKTEK BLOOD GLUCOSE METER, QUICKTEK BLOOD GLUCOSE STRIPS, QUICKTEK CONTROL SOLUTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010039
510(k) Type
Traditional
Applicant
Chronimed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2001
Days to Decision
217 days
Submission Type
Summary

QUICKTEK BLOOD GLUCOSE SYSTEM, QUICKTEK BLOOD GLUCOSE METER, QUICKTEK BLOOD GLUCOSE STRIPS, QUICKTEK CONTROL SOLUTION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010039
510(k) Type
Traditional
Applicant
Chronimed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/2001
Days to Decision
217 days
Submission Type
Summary