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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
FDA Hosted 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
FDA Hosted 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