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ARKRAY GLUCOCARD 01 BLOOD MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073416
510(k) Type
Traditional
Applicant
ARKRAY Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2008
Days to Decision
193 days
Submission Type
Summary

ARKRAY GLUCOCARD 01 BLOOD MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073416
510(k) Type
Traditional
Applicant
ARKRAY Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2008
Days to Decision
193 days
Submission Type
Summary