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ARKRAY GLUCOCARD 01 BLOOD GLUCOSE MONITORING SYSTEM AND RELION CONFIRM BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K124021
510(k) Type
Traditional
Applicant
Arkray Factory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
550 days
Submission Type
Summary

ARKRAY GLUCOCARD 01 BLOOD GLUCOSE MONITORING SYSTEM AND RELION CONFIRM BLOOD GLUCOSE MONITORING SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K124021
510(k) Type
Traditional
Applicant
Arkray Factory, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
550 days
Submission Type
Summary