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Assure Titanium 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
K200788
510(k) Type
Dual Track
Applicant
Arkray, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/23/2022
Days to Decision
788 days
Submission Type
Summary

Assure Titanium 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
K200788
510(k) Type
Dual Track
Applicant
Arkray, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/23/2022
Days to Decision
788 days
Submission Type
Summary