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ACCU-CHEK AVIVA EXPERT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K142089
510(k) Type
Traditional
Applicant
Roche Diagnostics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2014
Days to Decision
138 days
Submission Type
Summary

ACCU-CHEK AVIVA EXPERT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K142089
510(k) Type
Traditional
Applicant
Roche Diagnostics Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2014
Days to Decision
138 days
Submission Type
Summary