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cobas pulse 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
K220272
510(k) Type
Dual Track
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2024
Days to Decision
816 days
Submission Type
Summary

cobas pulse 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
K220272
510(k) Type
Dual Track
Applicant
Roche Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2024
Days to Decision
816 days
Submission Type
Summary