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