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ACCU-CHEK AVIVA EXPERT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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