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MODIFICATION TO TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER, TEST STRIPS AND GLUCOSE CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040670
510(k) Type
Special
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2004
Days to Decision
10 days
Submission Type
Statement

MODIFICATION TO TRUETRACK SMART SYSTEM BLOOD GLUCOSE METER, TEST STRIPS AND GLUCOSE CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040670
510(k) Type
Special
Applicant
HOME DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2004
Days to Decision
10 days
Submission Type
Statement