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GLUCOCARD 01-MINI BLOOD GLUCOSE MONITORING SYSTEM, MODEL 73110

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082417
510(k) Type
Special
Applicant
Arkray Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
60 days
Submission Type
Summary

GLUCOCARD 01-MINI BLOOD GLUCOSE MONITORING SYSTEM, MODEL 73110

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082417
510(k) Type
Special
Applicant
Arkray Factory USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2008
Days to Decision
60 days
Submission Type
Summary