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ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131366
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS OPERATIONS INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
151 days
Submission Type
Summary

ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131366
510(k) Type
Traditional
Applicant
ROCHE DIAGNOSTICS OPERATIONS INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
151 days
Submission Type
Summary