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Accu-Chek Safe-T-Pro Uno Lancing Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232509
510(k) Type
Traditional
Applicant
Roche Diabetes Care, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
87 days
Submission Type
Summary

Accu-Chek Safe-T-Pro Uno Lancing Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232509
510(k) Type
Traditional
Applicant
Roche Diabetes Care, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2023
Days to Decision
87 days
Submission Type
Summary