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Contour® next GEN Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193407
510(k) Type
Traditional
Applicant
Ascensia Diabetes Care
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2021
Days to Decision
745 days
Submission Type
Summary

Contour® next GEN Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193407
510(k) Type
Traditional
Applicant
Ascensia Diabetes Care
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2021
Days to Decision
745 days
Submission Type
Summary