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GLUCOCARD® W onyx 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
K183306
510(k) Type
Special
Applicant
ARKRAY Factory, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/10/2019
Days to Decision
133 days
Submission Type
Summary

GLUCOCARD® W onyx 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
K183306
510(k) Type
Special
Applicant
ARKRAY Factory, Inc.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/10/2019
Days to Decision
133 days
Submission Type
Summary